The present application is directed to interbody spinal fusion implants having a structural configuration that provides for the maintaining and creating of the normal anatomic angular relationship of two adjacent vertebrae of the spine to maintain and create spinal lordosis. The spinal fusion implants are sized to fit within the disc space created by the removal of disc material between two adjacent vertebrae and conform wholly or in part to the disc space created. The spinal fusion implants of the present invention have upper and lower surfaces that form a support structure for bearing against the end plates of the adjacent vertebrae. The upper and lower surfaces are disposed in a converging angular relationship to each other such that the implants have an overall “wedged-shape” in an elevational side view. The angular relationship of the upper and lower surfaces places and maintains the vertebrae adjacent to those surfaces in an angular relationship to each other, creating and maintaining the desired lordosis.

Patent
   7503933
Priority
Jun 07 1995
Filed
Sep 09 2002
Issued
Mar 17 2009
Expiry
Jun 07 2015
Assg.orig
Entity
Large
334
109
EXPIRED
245. An interbody spinal fusion implant for insertion into a recipient site formed at least in part within a disc space in between adjacent vertebral bodies of a human spine, said implant comprising:
a leading end for insertion first into the recipient site, a trailing end opposite said leading end and a mid-longitudinal axis through said leading and trailing ends, a depth along the mid-longitudinal axis, and a width and a height each perpendicular to the depth, said implant having a maximum width greater than the depth of said implant and greater than the height of said implant; and
a top and a bottom between said leading and trailing ends adapted to space apart the adjacent vertebral bodies, opposite sides between said top and said bottom, and between said leading and trailing ends, said top and said bottom each having a plurality of openings therethrough, said openings being in communication with one another to permit for the growth of bone from adjacent vertebral body to adjacent vertebral body through said implant, at least one of said openings being surrounded by said implant, said top and said bottom being in an angular relationship relative to the mid-longitudinal axis along at least a portion of the depth of said implant sufficient to maintain the adjacent vertebral bodies in an angular relationship to each other, said trailing end including a curved portion between said opposite sides to conform to the natural anatomical curvature of the adjacent vertebral bodies, said curved portion having a radius of curvature greater than a maximum dimension between said leading end and said trailing end along the mid-longitudinal axis of said implant, said leading end having a width between said opposite sides, said leading end being straight across a majority of the width of said leading end and across the mid-longitudinal axis of said implant.
1. An interbody spinal fusion implant for insertion into a recipient site formed at least in part within a disc space in between adjacent vertebral bodies of a human spine, said implant comprising:
a leading end for insertion first into the recipient site, a trailing end opposite said leading end and a mid-longitudinal axis through said leading and trailing ends, a depth along said mid-longitudinal axis, and a width and a height each perpendicular to the depth, said implant having a maximum width greater than the depth of said implant and greater than the height of said implant;
a top and a bottom between said leading and trailing ends adapted to space apart the adjacent vertebral bodies, said top and said bottom having at least one opening therethrough, said openings being in communication with one another to permit for the growth of bone from adjacent vertebral body to adjacent vertebral body through said implant, at least one of said openings being surrounded by said implant, said top and said bottom being in an angular relationship relative to the mid-longitudinal axis along at least a portion of the depth of said implant sufficient to maintain the adjacent vertebral bodies in an angular relationship to each other; and
opposite sides between said top and said bottom, and between said leading and trailing ends, said implant having a non-arcuate cross section through said top, bottom, and opposite sides transverse to the mid-longitudinal axis along at least a portion of the depth of said implant, said trailing end including a curved portion between said opposite sides to conform to the natural anatomical curvature of the adjacent vertebral bodies, said curved portion having a radius of curvature greater than a maximum dimension between said leading end and said trailing end along the mid-longitudinal axis of said implant, said leading end having a width between said opposite sides, said leading end being straight across a majority of the width of said leading end and across the mid-longitudinal axis of said implant.
116. An interbody spinal fusion implant for insertion into a recipient site formed in between adjacent vertebral bodies of a human spine, said implant comprising:
a leading end for insertion first into the recipient site, a trailing end opposite said leading end and a mid-longitudinal axis through said leading and trailing ends, a depth along said mid-longitudinal axis, and a width and a height each perpendicular to the depth, said implant having a maximum width greater than the depth of said implant and greater than the height of said implant;
a top and a bottom between said leading and trailing ends adapted to space apart the adjacent vertebral bodies, said top and said bottom having at least one opening therethrough, said openings being in communication with one another to permit for the growth of bone from adjacent vertebral body to adjacent vertebral body through said implant, at least one of said openings being surrounded by said implant, said top and said bottom being in an angular relationship relative to the mid-longitudinal axis along at least a portion of the depth of said implant sufficient to maintain the adjacent vertebral bodies in an angular relationship to each other; and
opposite sides between said top and said bottom, and between said leading and trailing ends, at least one of said opposite sides having at least one aperture in communication with said openings of said top and said bottom, said implant having a non-arcuate cross section through said top, bottom, and opposite sides transverse to the mid-longitudinal axis along at least a portion of the depth of said implant, said trailing end including a curved portion between said opposite sides to conform to the natural anatomical curvature of the adjacent vertebral bodies, said curved portion having a radius of curvature greater than a maximum dimension between said leading end and said trailing end along the mid-longitudinal axis of said implant, said leading end having a width between said opposite sides, said leading end being straight across a majority of the width of said leading end and across the mid-longitudinal axis of said implant.
2. The implant of claim 1, wherein each of said top and said bottom comprises an interior surface, said interior surfaces being spaced apart to define a hollow interior in communication with said openings.
3. The implant of claim 2, wherein said implant includes an access opening for accessing said hollow interior.
4. The implant of claim 3, wherein said access opening is larger than the largest of said openings.
5. The implant of claim 3, wherein said access opening is configured to permit insertion of osteogenic material into said hollow interior.
6. The implant of claim 5, wherein said osteogenic material includes a fusion promoting material.
7. The implant of claim 5, wherein said osteogenic material is bone.
8. The implant of claim 5, wherein said osteogenic material is a material other than bone.
9. The implant of claim 3, further comprising a cover for closing said access opening.
10. The implant of claim 9, wherein said cover cooperatively engages said access opening.
11. The implant of claim 10, wherein said cover comprises a slidable door.
12. The implant of claim 10, wherein said cover includes a surface deviation to facilitate opening and closing of said access opening with said cover.
13. The implant of claim 1, wherein said top and said bottom further comprise at least a second opening.
14. The implant of claim 1, wherein at least one of said openings are approximately 1 mm to 3 mm in diameter.
15. The implant of claim 1, wherein at least one of said openings is macroscopic in size.
16. The implant of claim 1, wherein at least one of said openings is microscopic in size.
17. The implant of claim 1, wherein at least one opening in said top and at least one opening in said bottom form a channel through said implant.
18. The implant of claim 1, wherein said trailing end includes at least one perforation.
19. The implant of claim 1, further comprising a plurality of openings capable of retaining fusion promoting material.
20. The implant of claim 19, wherein said plurality of openings comprise wells.
21. The implant of claim 1, wherein said sides have at least one aperture.
22. The implant of claim 21, wherein said at least one aperture is sized in the range of approximately 1 mm to 3 mm.
23. The implant of claim 21, wherein said at least one aperture is in communication with said openings in said top and said bottom.
24. The implant of claim 1, wherein said leading and trailing ends form junctions with said sides, the junctions of said sides and at least one of said trailing end and said leading end being rounded.
25. The implant of claim 1, wherein said sides are generally flat.
26. The implant of claim 1, wherein the shape of said sides is generally trapezoidal.
27. The implant of claim 1, wherein said implant is configured to generally taper from said trailing end to said leading end.
28. The implant of claim 1, wherein said implant is a wedge.
29. The implant of claim 1, wherein the width of said implant is approximately 32 mm for use in the lumbar spine.
30. The implant of claim 1, wherein the width of said implant is in the range of approximately 28 mm to 48 mm for use in the lumbar spine.
31. The implant of claim 1, wherein said implant has a generally rectangular cross section transverse to the mid-longitudinal axis along at least a portion of its depth.
32. The implant of claim 1, wherein said leading end is at least in part curved.
33. The implant of claim 1, wherein at least a portion of said leading end is tapered for facilitating insertion of said implant into the recipient site.
34. The implant of claim 1, wherein said trailing end is convex.
35. The implant of claim 1, wherein the maximum depth of said implant is less than the posterior to anterior depth of the end plates of the adjacent vertebral bodies.
36. The implant of claim 1, wherein said implant is adapted for insertion from a posterior aspect of the vertebral bodies.
37. The implant of claim 1, wherein said implant is adapted for insertion from an anterior aspect of the vertebral bodies.
38. The implant of claim 1, wherein said implant is sized to replace a substantial portion of the disc with a single implant.
39. The implant of claim 1, wherein said implant has substantially the same shape as a space created by the removal of at least a substantial portion of the nucleus pulposus and a portion of the annulus fibrosus from between the two adjacent vertebral bodies.
40. The implant of claim 1, wherein the height of said implant is substantially equal to the height of the space created by the removal of disc material from between the adjacent vertebral bodies.
41. The implant of claim 1, wherein said implant has substantially the same height, width and depth as a space created by the removal of at least generally the nucleus pulposus and at least a portion of the annulus fibrosus from between the two adjacent vertebral bodies.
42. The implant of claim 1, wherein said implant dimensionally corresponds to the space created by the removal of at least generally all of the nucleus pulposus and a portion of the annulus fibrosus when said adjacent vertebral bodies are distracted and placed in angular relationship to each other.
43. The implant of claim 1, wherein the depth of said implant is in the range of approximately 11 mm to 21 mm for use in the cervical spine.
44. The implant of claim 1, wherein the width of said implant is in the range of approximately 14 mm to 28 mm for use in the cervical spine.
45. The implant of claim 1, wherein said implant has a maximum height in the range of approximately 5 mm to 10 mm, and the maximum width of said implant is in the range of approximately 14 mm to 28 mm, and the depth of said implant is in the range of approximately 11 mm to 21 mm for use in the cervical spine.
46. The implant of claim 1 for use in the lumbar spine, wherein the depth of said implant is in the range of approximately 20 mm to 34 mm.
47. The implant of claim 1, wherein said implant has a maximum height in the range of approximately 8 mm to 16 mm, and the maximum width of said implant is in the range of approximately 28 mm to 48 mm, and the depth of said implant is in the range of approximately 20 mm to 34 mm for use in the lumbar spine.
48. The implant of claim 1, wherein the depth of said implant is substantially the same as the depth of a space created by the removal of the nucleus pulposus from between the two adjacent vertebral bodies.
49. The implant of claim 1, wherein the width of said implant is substantially equal to the transverse width of a space created by the removal of the nucleus pulposus from between the two adjacent vertebral bodies.
50. The implant of claim 1, wherein said top has a fixed shape which is generally configured to match the contours of the endplate of one of the two adjacent vertebral bodies.
51. The implant of claim 1, wherein said bottom has a fixed shape which is generally configured to match the natural contours of the endplate of one of the two adjacent vertebral bodies.
52. The implant of claim 1, further comprising at least one protrusion extending from said top and said bottom for engaging the adjacent vertebral bodies to maintain said implant within the disc space.
53. The implant of claim 52, wherein said protrusion comprises a ridge.
54. The implant of claim 52, wherein said protrusion comprises a plurality of ridges facing the same direction to prevent expulsion of said implant in a direction opposite to said same direction.
55. The implant of claim 52, wherein said protrusion comprises a tooth.
56. The implant of claim 52, wherein said protrusion comprises a ratchet.
57. The implant of claim 56, wherein said protrusion comprises a plurality of ratchets facing the same direction to prevent expulsion of said implant in a direction opposite to said same direction.
58. The implant of claim 1, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
59. The implant of claim 58, wherein said irregular surface comprises at least one groove.
60. The implant of claim 58, wherein said irregular surface includes knurling.
61. The implant of claim 58, wherein said irregular surface includes at least one spike.
62. The implant of claim 61, wherein said implant includes means for retracting and extending said at least one spike.
63. The implant of claim 1, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
64. The implant of claim 63, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
65. The implant of claim 63, wherein a height of each roughening measured from the mid-longitudinal axis of the implant decreases from said trailing end to said leading end.
66. The implant of claim 63, wherein said surface roughenings comprise at least one groove.
67. The implant of claim 1, wherein said top and said bottom have a bone ingrowth surface.
68. The implant of claim 1, wherein said implant has an exterior surface that is at least in part porous.
69. The implant of claim 1, wherein said implant comprises a mesh-like material having a plurality of interstices for receiving fusion promoting material.
70. The implant of claim 1, wherein said implant is porous.
71. The implant of claim 1, wherein said implant includes an exterior surface, at least a portion of which is treated to promote bone ingrowth between said surface and a vertebral body.
72. The implant of claim 1, in combination with a fusion promoting material other than bone in contact with said implant.
73. The implant of claim 1, wherein said implant comprises a bone ingrowth material other than bone.
74. The implant of claim 1, further comprising a material that intrinsically participates in the growth of bone from one of the adjacent vertebral bodies to the other of the adjacent vertebral bodies.
75. The implant of claim 1, wherein said implant is treated with a fusion promoting substance.
76. The implant of claim 75, wherein said fusion promoting substance is bone.
77. The implant of claim 1, wherein said implant is stronger than bone.
78. The implant of claim 1, in combination with an osteogenic material in contact with said implant.
79. The implant of claim 78, wherein said osteogenic material is a material other than bone.
80. The implant of claim 1, wherein said implant comprises a bone ingrowth material for promoting bone ingrowth between said implant and said two adjacent vertebral bodies.
81. The implant of claim 1, wherein said implant is at least in part bioresorbable.
82. The implant of claim 1, wherein said implant is adapted to be centrally placed within the disc space.
83. The implant of claim 1, wherein at least one of said leading and trailing ends of said implant is configured to engage a driving instrument for implanting said implant within the disc space between the two adjacent vertebral bodies.
84. The implant of claim 1, further comprising an expander moving said top and bottom apart in said diverging angular relationship.
85. The implant of claim 1, wherein said trailing end has a height greater than said leading end.
86. The implant of claim 1, wherein at least one of said top and bottom is substantially flat.
87. The implant of claim 86, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
88. The implant of claim 87, wherein said irregular surface comprises at least one groove.
89. The implant of claim 87, wherein said irregular surface includes knurling.
90. The implant of claim 86, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
91. The implant of claim 90, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
92. The implant of claim 1, wherein at least one of said top and bottom is generally planar.
93. The implant of claim 92, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
94. The implant of claim 93, wherein said irregular surface comprises at least one groove.
95. The implant of claim 93, wherein said irregular surface includes knurling.
96. The implant of claim 92, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
97. The implant of claim 96, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
98. The implant of claim 1, wherein each of said top and bottom are substantially flat.
99. The implant of claim 98, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
100. The implant of claim 99, wherein said irregular surface comprises at least one groove.
101. The implant of claim 99, wherein said irregular surface includes knurling.
102. The implant of claim 98, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
103. The implant of claim 102, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
104. The implant of claim 1, wherein each of said top and bottom are generally planar.
105. The implant of claim 104, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
106. The implant of claim 105, wherein said irregular surface comprises at least one groove.
107. The implant of claim 105, wherein said irregular surface includes knurling.
108. The implant of claim 104, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
109. The implant of claim 108, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
110. The implant of claim 1, wherein said implant has a generally quadrilateral cross section transverse to the mid-longitudinal axis along at least a portion of its depth.
111. The implant of claim 1, wherein the width of said implant is greater than one-half of the width of a disc space into which said implant is adapted to be inserted.
112. The implant of claim 1, wherein said implant is sized to replace a substantial portion of a spinal disc with a single implant.
113. The implant of claim 1, in combination with a fusion promoting substance in contact with said implant.
114. The implant of claim 113, wherein said fusion promoting substance includes at least one of bone, bone morphogenetic protein, hydroxyapatite, and hydroxyapatite tricalcium phosphate.
115. The implant of claim 1, in combination with an implant driver adapted to insert said implant into the implantation space.
117. The implant of claim 116, wherein each of said top and said bottom comprises an interior surface, said interior surfaces being spaced apart to define a hollow interior in communication with said openings.
118. The implant of claim 117, wherein said implant includes an access opening for accessing said hollow interior.
119. The implant of claim 118, wherein said access opening is larger than the largest of said openings.
120. The implant of claim 118, wherein said access opening is configured to permit insertion of osteogenic material into said hollow interior.
121. The implant of claim 120, wherein said osteogenic material includes a fusion promoting material.
122. The implant of claim 120, wherein said osteogenic material is bone.
123. The implant of claim 120, wherein said osteogenic material is a material other than bone.
124. The implant of claim 118, further comprising a cover for closing said access opening.
125. The implant of claim 124, wherein said cover cooperatively engages said access opening.
126. The implant of claim 125, wherein said cover comprises a slidable door.
127. The implant of claim 125, wherein said cover includes a surface deviation to facilitate opening and closing of said access opening with said cover.
128. The implant of claim 116, wherein said top and said bottom further comprise at least a second opening.
129. The implant of claim 116, wherein at least one of said openings are approximately 1 mm to 3 mm in diameter.
130. The implant of claim 116, wherein at least one of said openings is macroscopic in size.
131. The implant of claim 116, wherein at least one of said openings is microscopic in size.
132. The implant of claim 116, wherein at least one opening in said top and at least one opening in said bottom form a channel through said implant.
133. The implant of claim 116, wherein said trailing end includes at least one perforation.
134. The implant of claim 116, further comprising a plurality of openings capable of retaining fusion promoting material.
135. The implant of claim 134, wherein said plurality of openings comprise wells.
136. The implant of claim 116, wherein said at least one aperture is sized in the range of approximately 1 mm to 3 mm.
137. The implant of claim 116, wherein the junctions of said sides and at least one of said trailing end and said leading end are rounded.
138. The implant of claim 116, wherein said sides are generally flat.
139. The implant of claim 116, wherein the shape of said sides is generally trapezoidal.
140. The implant of claim 116, wherein said implant is configured to generally taper from said trailing end to said leading end.
141. The implant of claim 116, wherein said implant is a wedge.
142. The implant of claim 116, wherein the width of said implant is approximately 32 mm for use in the lumbar spine.
143. The implant of claim 116, wherein the width of said implant is in the range of approximately 28 mm to 48 mm for use in the lumbar spine.
144. The implant of claim 116, wherein said implant has a generally rectangular cross section transverse to the mid-longitudinal axis along at least a portion of its depth.
145. The implant of claim 116, wherein said leading end is at least in part curved.
146. The implant of claim 116, wherein at least a portion of said leading end is tapered for facilitating insertion of said implant into the recipient site.
147. The implant of claim 116, wherein said trailing end is convex.
148. The implant of claim 116, wherein the maximum depth of said implant is less than the posterior to anterior depth of the end plates of the adjacent vertebral bodies.
149. The implant of claim 116, wherein said implant is adapted for insertion from a posterior aspect of the vertebral bodies.
150. The implant of claim 116, wherein said implant is adapted for insertion from an anterior aspect of the vertebral bodies.
151. The implant of claim 116, wherein said implant is sized to replace a substantial portion of a spinal disc with a single implant.
152. The implant of claim 116, wherein said implant has substantially the same shape as a space created by the removal of at least a substantial portion of the nucleus pulposus and a portion of the annulus fibrosus from between the two adjacent vertebral bodies.
153. The implant of claim 116, wherein the height of said implant is substantially equal to the height of the space created by the removal of disc material from between the adjacent vertebral bodies.
154. The implant of claim 116, wherein said implant has substantially the same height, width and depth as a space created by the removal of at least generally the nucleus pulposus and at least a portion of the annulus fibrosus from between the two adjacent vertebral bodies.
155. The implant of claim 116, wherein said implant dimensionally corresponds to the space created by the removal of at least generally all of the nucleus pulposus and a portion of the annulus fibrosus when said adjacent vertebral bodies are distracted and placed in angular relationship to each other.
156. The implant of claim 116, wherein the depth of said implant is in the range of approximately 11 mm to 21 mm for use in the cervical spine.
157. The implant of claim 116, wherein the width of said implant is in the range of approximately 14 mm to 28 mm for use in the cervical spine.
158. The implant of claim 116, wherein said implant has a maximum height in the range of approximately 5 mm to 10 mm, and the maximum width of said implant is in the range of approximately 14 mm to 28 mm, and the depth of said implant is in the range of approximately 11 mm to 21 mm for use in the cervical spine.
159. The implant of claim 116, for use in the lumbar spine, wherein the depth of said implant is in the range of approximately 20 mm to 34 mm.
160. The implant of claim 116, wherein said implant has a maximum height in the range of approximately 8 mm to 16 mm, and the maximum width of said implant is in the range of approximately 28 mm to 48 mm, and the depth of said implant is in the range of approximately 20 mm to 34 mm for use in the lumbar spine.
161. The implant of claim 116, wherein the depth of said implant is substantially the same as the depth of a space created by the removal of the nucleus pulposus from between the two adjacent vertebral bodies.
162. The implant of claim 116, wherein the width of said implant is substantially equal to the transverse width of a space created by the removal of the nucleus pulposus from between the two adjacent vertebral bodies.
163. The implant of claim 116, wherein said top has a fixed shape which is generally configured to match the contours of the endplate of one of the two adjacent vertebral bodies.
164. The implant of claim 116, wherein said bottom has a fixed shape which is generally configured to match the natural contours of the endplate of one of the two adjacent vertebral bodies.
165. The implant of claim 116, further comprising at least one protrusion extending from said top and said bottom for engaging the adjacent vertebral bodies to maintain said implant within the disc space.
166. The implant of claim 165, wherein said protrusion comprises a ridge.
167. The implant of claim 165, wherein said protrusion comprises a plurality of ridges facing the same direction to prevent expulsion of said implant in a direction opposite to said same direction.
168. The implant of claim 165, wherein said protrusion comprises a tooth.
169. The implant of claim 165, wherein said protrusion comprises a ratchet.
170. The implant of claim 169, wherein said protrusion comprises a plurality of ratchets facing the same direction to prevent expulsion of said implant in a direction opposite to said same direction.
171. The implant of claim 116, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
172. The implant of claim 171, wherein said irregular surface comprises at least one groove.
173. The implant of claim 171, wherein said irregular surface includes knurling.
174. The implant of claim 171, wherein said irregular surface includes at least one spike.
175. The implant of claim 174, wherein said implant includes means for retracting and extending said at least one spike.
176. The implant of claim 116, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
177. The implant of claim 176, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
178. The implant of claim 176, wherein a height of each roughening measured from the mid-longitudinal axis of the implant decreases from said trailing end to said leading end.
179. The implant of claim 176, wherein said surface roughenings comprise at least one groove.
180. The implant of claim 116, wherein said top and said bottom have a bone ingrowth surface.
181. The implant of claim 116, wherein said implant has an exterior surface that is at least in part porous.
182. The implant of claim 116, wherein said implant comprises a mesh-like material having a plurality of interstices for receiving fusion promoting material.
183. The implant of claim 116, wherein said implant is porous.
184. The implant of claim 116, wherein said implant includes an exterior surface, at least a portion of which is treated to promote bone ingrowth between said surface and a vertebral body.
185. The implant of claim 116, in combination with a fusion promoting material other than bone in contact with said implant.
186. The implant of claim 116, wherein said implant comprises a bone ingrowth material other than bone.
187. The implant of claim 116, further comprising a material that intrinsically participates in the growth of bone from one of the adjacent vertebral bodies to the other of the adjacent vertebral bodies.
188. The implant of claim 116, wherein said implant is treated with a fusion promoting substance.
189. The implant of claim 188, wherein said fusion promoting substance is bone.
190. The implant of claim 116, wherein said implant is stronger than bone.
191. The implant of claim 116, in combination with an osteogenic material in contact with said implant.
192. The implant of claim 191, wherein said osteogenic material is a material other than bone.
193. The implant of claim 116, wherein said implant comprises a bone ingrowth material for promoting bone ingrowth between said implant and said two adjacent vertebral bodies.
194. The implant of claim 116, wherein said implant is at least in part bioresorbable.
195. The implant of claim 116, wherein said implant is adapted to be centrally placed within a disc space.
196. The implant of claim 116, wherein at least one of said leading and trailing ends of said implant is configured to engage a driving instrument for implanting said implant within the disc space between the two adjacent vertebral bodies.
197. The implant of claim 116, further comprising an expander moving said top and bottom apart in said diverging angular relationship.
198. The implant of claim 116, wherein said trailing end has a height greater than said leading end.
199. The implant of claim 116, wherein at least one of said top and bottom is substantially flat.
200. The implant of claim 199, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
201. The implant of claim 200, wherein said irregular surface comprises at least one groove.
202. The implant of claim 200, wherein said irregular surface includes knurling.
203. The implant of claim 199, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
204. The implant of claim 203, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
205. The implant of claim 116, wherein at least one of said top and bottom is generally planar.
206. The implant of claim 205, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
207. The implant of claim 206, wherein said irregular surface comprises at least one groove.
208. The implant of claim 206, wherein said irregular surface includes knurling.
209. The implant of claim 205, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
210. The implant of claim 209, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
211. The implant of claim 116, wherein each of said top and bottom are substantially flat.
212. The implant of claim 211, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
213. The implant of claim 212, wherein said irregular surface comprises at least one groove.
214. The implant of claim 212, wherein said irregular surface includes knurling.
215. The implant of claim 211, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
216. The implant of claim 215, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
217. The implant of claim 116, wherein each of said top and bottom are generally planar.
218. The implant of claim 217, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
219. The implant of claim 218, wherein said irregular surface comprises at least one groove.
220. The implant of claim 218, wherein said irregular surface includes knurling.
221. The implant of claim 217, further comprising a plurality of surface roughenings for engaging said adjacent vertebral bodies and for maintaining said implant in place, said surface roughenings being present on at least a portion of said top and said bottom.
222. The implant of claim 221, wherein said roughenings cover substantially the entire top and bottom of said implant, said roughenings being generally tapered from said trailing end to said leading end.
223. The implant of claim 116, wherein said implant has a generally quadrilateral cross section transverse to the mid-longitudinal axis along at least a portion of its depth.
224. The implant of claim 116, wherein the width of said implant is greater than one-half of the width of the disc space into which said implant is adapted to be inserted.
225. The implant of claim 116, wherein said implant is sized to replace a substantial portion of a spinal disc with a single implant.
226. The implant of claim 116, in combination with a fusion promoting substance in contact with said implant.
227. The implant of claim 226, wherein said fusion promoting substance includes at least one of bone, bone morphogenetic protein, hydroxyapatite, and hydroxyapatite tricalcium phosphate.
228. The implant of claim 116, in combination with an implant driver adapted to insert said implant into the implantation space.
229. The implant of claim 1, wherein said implant is sized to be wholly contained within the recipient site.
230. The implant of claim 116, wherein said implant is sized to be wholly contained within the recipient site.
231. The implant of claim 3, wherein said leading end includes said access opening.
232. The implant of claim 13, wherein at least two of said openings are of different sizes.
233. The implant of claim 1, wherein said implant is made at least in part of metal.
234. The implant of claim 1, wherein said trailing end is curved along a portion of said trailing end across the mid-longitudinal axis of said implant.
235. The implant of claim 1, wherein said trailing end is curved across the entire width of said implant.
236. The implant of claim 1, wherein at least one of said top and said bottom includes a portion extending across the entire depth of said implant generally halfway between said opposite sides.
237. The implant of claim 1, wherein said at least one opening has a central longitudinal axis and a maximum dimension transverse to the central longitudinal axis, the maximum dimension of said at least one opening being less than the maximum width of said implant.
238. The implant of claim 118, wherein said leading end includes said access opening.
239. The implant of claim 128, wherein at least two of said openings are of different sizes.
240. The implant of claim 116, wherein said implant is made at least in part of metal.
241. The implant of claim 116, wherein said trailing end is curved along a portion of said trailing end across the mid-longitudinal axis of said implant.
242. The implant of claim 116, wherein said trailing end is curved across the entire width of said implant.
243. The implant of claim 116, wherein at least one of said top and said bottom includes a portion extending across the entire depth of said implant generally halfway between said opposite sides.
244. The implant of claim 116, wherein said at least one opening has a central longitudinal axis and a maximum dimension transverse to the central longitudinal axis, the maximum dimension of said at least one opening being less than the maximum width of said implant.
246. The implant of claim 245, wherein each of said top and said bottom comprises an interior surface, said interior surfaces being spaced apart to define a hollow interior in communication with said openings.
247. The implant of claim 245, wherein said implant is a wedge.
248. The implant of claim 245, wherein said implant has a generally quadrilateral cross section transverse to the mid-longitudinal axis along at least a portion of its depth.
249. The implant of claim 245, wherein said implant has a generally rectangular cross section transverse to the mid-longitudinal axis along at least a portion of its depth.
250. The implant of claim 245, wherein said trailing end has a height greater than said leading end.
251. The implant of claim 245, further comprising at least one protrusion extending from said top and said bottom for engaging the adjacent vertebral bodies to maintain said implant within the disc space.
252. The implant of claim 251, wherein said protrusion comprises at least one of a ridge, a tooth, and a ratchet.
253. The implant of claim 251, wherein said protrusion comprises a plurality of ratchets facing the same direction to prevent expulsion of said implant in a direction opposite to said same direction.
254. The implant of claim 245, further comprising an irregular surface for engaging the adjacent vertebral bodies and for maintaining said implant in place, said irregular surface being present on at least a part of said top and said bottom.
255. The implant of claim 254, wherein said irregular surface comprises at least one groove.
256. The implant of claim 254, wherein said irregular surface includes knurling.
257. The implant of claim 245, wherein said implant is at least in part bioresorbable.
258. The implant of claim 245, in combination with a fusion promoting substance in contact with said implant.
259. The implant of claim 258, wherein said fusion promoting substance includes at least one of bone, bone morphogenetic protein, hydroxyapatite, and hydroxyapatite tricalcium phosphate.
260. The implant of claim 245, wherein at least two of said openings are of different sizes.
261. The implant of claim 245, wherein at least one of said top and said bottom includes a portion extending across the entire depth of said implant generally halfway between said opposite sides.
262. The implant of claim 245, wherein said trailing end is at least in part convex.
263. The implant of claim 245, wherein said trailing end is curved along a portion of said trailing end across the mid-longitudinal axis of said implant.
264. The implant of claim 245, wherein said trailing end is curved across the entire width of said implant.
265. The implant of claim 245, wherein at least one of said plurality of openings has a central longitudinal axis and a maximum dimension transverse to the central longitudinal axis, the maximum dimension of said at least one of said plurality of openings being less than the maximum width of said implant.
266. The implant of claim 245, wherein said implant has a non-arcuate cross section through said top and bottom transverse to the mid-longitudinal axis along at least a portion of the depth of said implant.
267. The implant of claim 1, wherein said opposite sides are at least in part parallel to one another.
268. The implant of claim 116, wherein said opposite sides are at least in part parallel to one another.
269. The implant of claim 1, wherein said trailing end includes a portion in a plane being at an acute angle to both said top and said bottom.
270. The implant of claim 116, wherein said trailing end includes a portion in a plane being at an acute angle to both said top and said bottom.
271. The implant of claim 245, wherein said trailing end includes a portion in a plane being at an acute angle to both said top and said bottom.
272. The implant of claim 245, wherein said implant is made at least in part of metal.
273. The implant of claim 3, wherein said access opening and said at least one opening of said top and said bottom each have a shape, the shape of said access opening being different than the shape of said at least one opening of said top and said bottom.
274. The implant of claim 118, wherein said access opening and said at least one opening of said top and said bottom each have a shape, the shape of said access opening being different than the shape of said at least one opening of said top and said bottom.
275. The implant of claim 245, wherein said implant includes a hollow interior in communication with said openings.
276. The implant of claim 275, wherein said implant includes an access opening for accessing said hollow interior.
277. The implant of claim 276, wherein said access opening and said plurality of openings each have a shape, the shape of said access opening being different than the shape of said plurality of openings.

This is a continuation of application Ser. No. 09/412,090, filed Oct. 4, 1999, now U.S. Pat. No. 6,441,544; which is a continuation of application Ser. No. 08/813,283, filed Mar. 10, 1997, now U.S. Pat. No. 6,302,914; which is a divisional of application Ser. No. 08/482,146, filed Jun. 7, 1995, now U.S. Pat. No. 5,609,635; all of which are incorporated herein by reference.

1. Field of the Invention

The present invention relates generally to interbody spinal fusion implants, and in particular to spinal fusion implants configured to restore and maintain two adjacent vertebrae of the spine in correct anatomical angular relationship.

2. Description of The Related Art

Both the cervical and lumbar areas of the human spine are, in a healthy state, lordotic such that they are curved convex forward. It is not uncommon that in degenerative conditions of the spine that lordosis is lost. This effectively shortens the spinal canal which decreases its capacity. Further, the absence of lordosis moves the spinal cord anteriorly where it may be compressed against the posterior portions of the vertebral bodies and discs. Finally, such a loss of lordosis disturbs the overall mechanics of the spine which may cause cascading degenerative changes throughout the adjacent spinal segments.

The surgical treatment of those degenerative conditions of the spine in which the spinal discs are in various states of collapse, and out of lordosis, commonly involves spinal fusion. That is the joining together of adjacent vertebrae through an area of shared bone. When the shared bone is in the area previously occupied by the intervertebral disc that is referred to as an interbody fusion. Further history in this regard is provided in application Ser. No. 08/263,952 entitled Artificial Spinal Fusion Implants (“Parent Application”) incorporated herein by reference.

The Parent Application taught the use of artificial spinal fusion implants that were capable of being placed between adjacent vertebrae, and which implants were capable of containing and providing fusion promoting substances including bone at the fusion site. These devices were further capable of restoring the height of the disc space and of supporting the spine, and were self-stabilizing as well as being stabilizing to the spinal area where implanted.

The present invention is directed to interbody spinal fusion implants having a structural configuration that provides for the maintaining and creating of the normal anatomic angular relationship of two adjacent vertebrae of the spine to maintain and create spinal lordosis. The spinal fusion implants of the present invention are sized to fit within the disc space created by the removal of disc material between two adjacent vertebrae and conform wholly or in part to the disc space created. The spinal fusion implants of the present invention have upper and lower surfaces that form a support structure for bearing against the end plates of the adjacent vertebrae. In the preferred embodiments, the upper and lower surfaces are disposed in a converging angular relationship to each other such that the implants of the present invention have an overall “wedged-shape” in an elevational side view. The angular relationship of the upper and lower surfaces places and maintains the vertebrae adjacent to those surfaces in an angular relationship to each other, creating and maintaining the desired lordosis.

The implants of the present invention may have surface irregularities to increase their surface area, and/or to further engage the adjacent vertebrae and to enhance stability. The lordotic implants of the present invention may have surface irregularities that are uniform in height along the longitudinal axis of the upper and lower vertebrae engaging surfaces, or may increase in height from one end of the implant to the other. That is, the implant body and the surface formed and the projections may be similarly wedged. The outer contour of the surface projections may be more or less rectangular while the underlying implant may be wedge-shaped; or the reverse wherein the underlying implant body is more or less rectangular while the contour of the surface projections are wedge-shaped from one end of the implant to the other.

The implants of the present invention have various faces which may be curved so as to conform to the shape of the vertebral surfaces adjacent to the area of the disc removal. Specifically the upper and/or lower surfaces may be convex, and/or the front and/or rear surfaces may be convex. The surfaces of the implants of the present invention may have openings which may or may not pass all the way through them, and a central chamber in communication to the surface through holes. The openings may be of random sizes, and/or shapes, and/or distributions. The implants themselves may be composed of materials, and/or have surface treatments, to encourage microscopic bone ingrowth into the implants.

In the performing of a posterior lumbar interbody fusion, it is not possible to replace the removed portions of the disc, if a total nuclear discectomy has been performed, with a single large implant as the delicate dural sac containing the spinal cord, and the nerve roots cover at all times at least some portion of the posterior disc space. As set forth in the Parent Application, the use of “modular implants” is appropriate in such cases. The modular implants being approximately as long as the depth of the disc material removed, but being considerably narrower, such that they can be introduced into the disc space from the posterior aspect to either side of the dural sac, and then aligned side to side within the disc space so that a number of them each having a length consistent with the depth of the disc removed in that area would in combination have a width equal to the width of the disc material removed.

The modular implants of the present invention may be generally wedge-shaped and may have upper and lower surfaces conforming to the contours of the vertebral endplates, which contours include but are not limited to being relatively flat or convex. As the disc spaces in the lumbar spine are generally lordotic, said implants in the preferred embodiment would be taller anteriorly, that is at the implant's insertion end, and less tall posteriorly, that is at the implant's trailing end. To introduce an implant that is taller at its insertion end than the space available at the posterior aspect of the disc space, even when that disc space is optimally distracted, is problematic.

The modular implants of the present invention provide two solutions to the problem. In the first embodiment, the modular implants may have a reduced size at their insertion end, including but not limited to a bullet nose, a convexity, and a chamfer to a smaller front surface. This then provides that the implant has an area small enough to be introduced into the posterior aspect of the disc space when the disc space is adequately distracted and the contour of that specialized leading portion of the implant is such that it then allows for a ramping up of the adjacent vertebrae relative to the implant as the implant is advanced forward into the disc space.

The implants of the present invention provide a second solution to this same problem. In the preferred embodiment of the modular implant, the implant is again wedge-shaped in the side elevational view and is taller at its insertion end than at its trailing end. However, the implant incorporates at its trailing end a means for engaging insertion instrumentation such as the box and threaded opening configuration disclosed in the Parent Application. Since in the preferred embodiment these implants are wedge-shaped in the side elevational view when upright but are generally rectangular when viewed from the top plan view, these implants are therefore designed to be introduced into the disc space on their side such that the side walls of the implants are adjacent to the end plates of the adjacent vertebrae. The implants have a side-to-side dimension that is less than the dimension through the insertion end of the implant when upright. It is possible to easily insert these implants with them on their side and then to use the insertion instrument engaged to the implant to rotate the implants ninety degrees into the fully upright position, once they have been fully inserted. Once inserted, the upper and lower surfaces are adjacent to the endplates of the adjacent vertebrae and create and maintain the desired angular relationship of the adjacent vertebrae as the upper and lower walls are angled with respect to each other.

In an alternative embodiment of the present invention, a mechanical implant which may be inserted in a collapsed position and which may then be adjusted to increase in height so as to provide for the optimal restoration of the height of the space between the adjacent vertebrae is disclosed. The mechanical implant may be wedge-shaped, and have upper and lower surfaces, the contours of which generally conform to the contacted areas of the adjacent vertebral endplates and which contours may include but are not limited to being relatively flat, or convex. Further, the mechanical implant may be wedge-shaped or generally rectangular, but capable of increasing in both height and the extent of wedging when adjusted. This may easily be achieved by having one of the two wedge mechanisms employed in the example given being larger, or steeper than the other. Alternatively, a single wedge may be utilized, and if it is desired to achieved increased height at one end of the implant while restricting the height at the other, then the end of the implant may incorporate a hinge means and the height expansion at the other end achieved by drawing a wedge member, bar, ball, or other means from the far end toward the hinged end so as to drive said upper and lower surfaces apart in a wedged fashion.

In an alternative embodiment of the present invention, an implant having a mechanically deployable bone engaging means is taught. Such an implant is generally wedge-shaped in the side elevational view and has upper and lower surfaces generally conforming to the contour of the vertebral endplates where contacted by the implant, and which upper and lower surfaces may be but are not limited to being either flat or convex. The use of such deployable bone engaging means are particularly of value in that the largest possible implant may be inserted into a disc space and the vertebral engaging means, which if fixed to the surface would have blocked the insertion of the implant, may then be deployed after the insertion such that the distance from the tip of the upper and lower bone engagement means exceeds the height of the space available for insertion. Such a feature is of particular value when the implant itself is wedge-shaped as the considerable compressive loads across the lumbar spine would tend to drive a wedge-shaped implant out of the disc space.

It is an object of the present invention to provide a spinal fusion implant that is easily inserted into the spine, having a tapered leading end;

It is another object of the present invention to provide a spinal fusion implant that tapers in height from one end to the other consistent with the taper of a normal spinal disc;

It is yet another object of the present invention to provide a spinal fusion implant that is capable of maintaining anatomic alignment and lordosis of two adjacent vertebrae during the spinal fusion process;

It is still another object of the present invention to provide a spinal fusion implant that is self stabilizing within the spine;

It is yet another object of the present invention to provide a spinal fusion implant that is capable of providing stability between adjacent vertebrae when inserted;

It is further another object of the present invention to provide a spinal fusion implant that is capable of spacing apart and supporting adjacent vertebrae in an angular relationship during the spinal fusion process;

It is still further another object of the present invention to provide a spinal fusion implant that fits between to adjacent vertebrae and preserves the end plants of those vertebrae; and

It is another object of the present invention to provide a spinal fusion implant having a shape which conforms to the endplates of the adjacent vertebrae; and

These and other objects of the present invention will become apparent from a review of the accompanying drawings and the detailed description of the drawings.

FIG. 1 is a perspective view of the lordotic interbody spinal fusion implant of the present invention with a slidable door shown in a partially open position providing access to the internal chamber of the implant.

FIG. 2 is a top plan view of the lordotic interbody spinal fusion implant of the present invention.

FIG. 3 is a left side elevational view of the lordotic interbody spinal fusion implant of the present invention.

FIG. 4 is a right side elevational view of the lordotic interbody spinal fusion implant of the present invention.

FIG. 5 is a front end view of the lordotic interbody spinal fusion implant of the present invention showing the slidable door in a partially open position.

FIG. 6 is a rear end view of the lordotic interbody spinal fusion implant of the present invention showing the means for engaging insertion instrumentation.

FIG. 7 is an enlarged fragmentary view along line 7 of FIG. 2 illustrating the bone engaging surface configuration of the lordotic interbody spinal fusion implant of the present invention.

FIG. 7A is an elevational side view of a segment of the spinal column having the lordotic implant of the present invention inserted in the disc space at different disc levels between adjacent vertebrae to restore and maintain the correct anatomical alignment of the adjacent vertebrae.

FIG. 8 is a top plan view of an alternative embodiment of the lordotic interbody spinal fusion implant of the present invention.

FIG. 9 is a left side elevational view of the lordotic interbody spinal fusion implant of FIG. 8.

FIG. 10 is a front end view of the lordotic interbody spinal fusion implant of FIG. 8.

FIG. 11 is a rear end view of the lordotic interbody spinal fusion implant of FIG. 8 showing the means for engaging insertion instrumentation.

FIG. 12 is an enlarged fragmentary view along line 12 of FIG. 8 illustrating the surface configuration the lordotic interbody spinal fusion implant of the present invention.

FIG. 13 is a top plan view of an alternative embodiment of the lordotic interbody spinal fusion implant of the present invention made of a mesh-like material.

FIG. 14 is a left side elevational view of the lordotic interbody spinal fusion implant of FIG. 13.

FIG. 15 is a front end view of the lordotic interbody spinal fusion implant of FIG. 13.

FIG. 16 is a rear end view of the lordotic interbody spinal fusion implant of FIG. 13 showing the means for engaging insertion instrumentation.

FIG. 17 is an enlarged fragmentary view along line 17 of FIG. 13 illustrating the surface configuration of the lordotic interbody spinal fusion implant of the present invention.

FIG. 18 is a perspective view of an alternative embodiment of the lordotic interbody spinal fusion implant of the present invention.

FIG. 19 is a top plan view of the lordotic interbody spinal fusion implant of FIG. 18.

FIG. 20 is a left side elevational view of the lordotic interbody spinal fusion implant of FIG. 18.

FIG. 21 is a rear end view of the lordotic interbody spinal fusion implant of FIG. 18.

FIG. 22 is a front end view of the lordotic interbody spinal fusion implant of FIG. 18.

FIG. 23 is an enlarged fragmentary view along line 23 of FIG. 22 illustrating the surface configuration the lordotic interbody spinal fusion implant of the present invention.

FIG. 24 is a top plan view of an alternative embodiment of the lordotic interbody spinal fusion implant of the present invention.

FIG. 25 is a left side elevational view of the lordotic interbody spinal fusion implant of FIG. 24.

FIG. 26 is a rear end view of the lordotic interbody spinal fusion implant of FIG. 24.

FIG. 27 is a front end view of the lordotic interbody spinal fusion implant of FIG. 24.

FIG. 28 is an enlarged fragmentary view along line 28 of the lordotic interbody spinal fusion implant of FIG. 24 illustrating the surface configuration of the lordotic interbody spinal fusion implant of the present invention.

FIG. 29 is a sectional view along lines 29-29 of FIG. 28 the lordotic interbody spinal fusion implant of the present invention.

FIG. 30 is a side elevational view of a segment of the human spinal column shown with an alternative embodiment of the lordotic spinal fusion implant of the present invention that is adjustable and expandable shown in sectional view inserted in the disc space levels to restore and maintain the correct anatomical alignment of the adjacent vertebrae.

FIG. 31 is a side cross sectional view of, an alternative embodiment of the lordotic implant of the present invention having movable projections, in the form of spikes 708, which are movable from a first position within the implant 700 to a second position extending to the exterior of the implant.

FIG. 32 is a perspective view of the embodiment of FIG. 31.

Referring to FIGS. 1 through 7 the lordotic interbody spinal fusion implant of the present invention for use in the disc space between two adjacent vertebrae, generally referred to by the numeral 100, is shown. The implant 100 has a generally rectangular configuration, having an upper surface 112 and a lower surface 114. In the preferred embodiment, the upper and lower surfaces 112 and 114 of implant 100 are disposed in a converging angular relationship toward each other such that the implant 100 appears “wedge-shaped” from a side elevational view as shown in FIGS. 3 and 4. The upper and lower surfaces 112 and 114 have an interior surface which form a support structure for bearing against the endplates of the adjacent vertebrae between which the implant 100 is inserted. The angular relationship of the upper and lower surfaces 112 and 114 places and maintains the vertebrae adjacent to those surfaces in an angular relationship, creating and maintaining the desired lordosis of the spine.

The upper and lower surfaces 112 and 114 of the implant 100 may be flat or curved to conform to the shape of the end plates of the adjacent vertebrae between which the implant 100 is inserted. The implant 100 conforms to the shape of the nucleus pulposus and a portion of the annulus fibrosus removed from the vertebrae. The upper and lower surfaces 112 and 114 comprise surface roughenings that provide a surface suitable for engaging the adjacent vertebrae to stabilize the implant 100 within the disc space once surgically implanted. The surface roughenings of the upper and lower surfaces 112 and 114 comprise a surface knurling 121 and/or grooves.

Referring to FIG. 7, an enlarged fragmentary view of the surface knurling 121 of the implant 100 is shown as a diamond-shaped bone engaging pattern. The implant 100 may have surface knurling 121 throughout the entire upper and lower surfaces 112 and 114, throughout only a portion of the upper and lower surfaces 112 and 114, or any combination thereof, without departing from the scope of the present invention. It is also appreciated that the surface knurling 121 may have various configuration other than the configuration shown.

In this embodiment, the implant 100 is hollow and comprises a plurality of openings 115 of passing through the upper and lower surfaces 112 and 114 and into a central hollow chamber 116. The openings 115 provide for bone growth to occur from the vertebrae through the openings 115 to the internal chamber 116. While the openings 115 have been shown in the drawings as being circular, it is appreciated that the openings 115 may have any shape, size, configuration or distribution suitable for use in a spinal implant without departing from the scope of the present invention. For example, the openings may have a tear-drop configuration as shown in opening 115a in FIGS. 1 and 2. The upper and lower surfaces 112 and 114 of the implant 100 are supported and spaced apart by a side wall 118, which may also comprise a plurality of openings 122.

The implant 100 has an insertion end 120 and a trailing end 130 both of which may be curved or flat. The trailing end 130 of the implant may be convex to conform to the curvature of the vertebrae and has a means for engaging an implant insertion instrument comprising a depressed portion 124 with a central threaded opening 126 for receiving the engaging end of a driving instrument. The insertion end 120 of the implant 100 comprises an access opening 132 and a slidable door 134 which closes the opening 132. The slidable door 134 covers the opening 132 into the chamber 116 and permits the insertion of autogenous bone material into the chamber 116.

In use, the slidable door 134 is placed in the open position for loading material into the chamber 116. The slideable door 134 has a depression 136 for facilitating the opening and closing of the door 134. The internal chamber 116 can be filled and hold any natural or artificial osteoconductive, osteoinductive, osteogenic, or other fusion enhancing material. Some examples of such materials are bone harvested from the patient, or bone growth inducing material such as, but not limited to, hydroxyapatite, hydroxyapatite tricalcium phosphate; or bone morphogenic protein. The implant 100 itself is made of material appropriate for human implantation such as titanium and/or may be made of, and/or filled and/or coated with a bone ingrowth inducing material such as, but not limited to, hydroxyapatite or hydroxyapatite tricalcium phosphate or any other osteoconductive, osteoinductive, osteogenic, or other fusion enhancing material.

The fusion enhancing material that is packed within the chamber 116 of the implant 100 serves to promote bone ingrowth between the implant 100 and the adjacent vertebrae. Once the bone ingrowth occurs, the implant 100 will be a permanent fixture preventing dislodgement of the implant as well as preventing any movement between the adjacent vertebrae.

The slidable door 134 is then closed prior to implantation. In the closed position, the slideable door conforms to the curvature of the insertion end 120 of the implant 100. Various methods of packing the implant 100 with the autogenous bone material may be used to obtain a completely packed implant 100.

The method of inserting the implant 100 is set forth in detail in application Ser. No. 08/263,952, incorporated herein by reference. The threaded end of a driving instrument is attached to the threaded opening 126 in the trailing end 130 of the implant 100 and the fitting of the driving instrument into the depressed portion 124 prevents movement of the implant 100 in relationship to the driving instrument. The implant 100 is then placed at the entrance to the disc space between the two adjacent vertebrae V. The driver instrument is then tapped with a hammer sufficiently hard enough to drive the implant 100 into the disc space.

The size of the implant 100 is substantially the same size as the disc material that it is replacing and thus will be larger or smaller depending on the amount of disc material removed to create the disc space in which it is to be used. In the preferred embodiment in regard to the lumbar spine the implant 100 has a width W approximately 28-48 mm wide, approximately 36 mm being preferred. The implant 100 has a height H conforming to the restoration of the anatomic height of the disc space the average height would range from 8-16 mm, with 10-12 of which being the preferred average height. The depth D along mid-longitudinal axis MLA would at its maximum range from 20 to 34 mm with 26 to 32 being the preferred maximum depth. In the cervical spine the width of the implant is in the range of approximately 14-28 mm, with the preferred width being 18-22 mm. The implant has a height in the range of approximately 5-10 mm with the preferred height being 6-8 mm. The implant has a depth in the range of approximately 11-21 mm with the preferred depth being 11-13 mm.

Referring to FIG. 7A, a side elevational view of the lateral aspect of a segment of the spinal column S is shown with the implant 100 inserted in the disc space D2 between two adjacent vertebrae V2 and V3. The implant 100 is inserted in the direction of arrow A into the disc space D2 and maintains the two vertebrae V2 and V3 in angular relationship to each other such that the natural lordosis of that segment of the spinal column S is restored. The forward advancement of the implant 100 is blocked by the natural bone processes B in the endplates of the vertebrae V2 and V3. Backing out of the implant 100 is prevented by the bone engaging surface knurling 121 of the upper and lower surfaces 112 and 114.

Referring to FIG. 8-12, an alternative embodiment of the lordotic interbody spinal fusion implant of the present invention, generally referred to by the numeral 200, is shown. The implant 200 has a similar overall configuration as the implant 100 described above. In the preferred embodiment, the implant 200 is solid and comprises a plurality of channels 215 passing from the upper surface 212 to the lower surface 214 through the implant 200. The channels 215 provide for bone ingrowth and facilitate the incorporation of the implant 200 into the spinal fusion mass. The channels may also be loaded with fusion promoting materials such as those described above, prior to implantation. It is appreciated that the channels 215 need not pass all the way through the implant 200, but can have a configuration similar to wells, which may hold fusion promoting materials and permit bone ingrowth into the upper and lower surfaces 212 and 214 of the implant 200.

In addition to the channels 215, the implant 200 may have small openings 222 on the side wall 218 which may or may not pass through the entire implant 200. The same openings 222 may be in communication with the channels 215 such that bone ingrowth may occur from the openings 222 to the channels 215 to lock the implant 200 into the fusion mass. If the openings 222 do not pass through the entire implant 200, they may function as small wells for holding fusion promoting materials or described above.

In the preferred embodiment of implant 200, the channels 215 have a diameter in the range of 0.1 mm to 6 mm, with 2-3 mm being the preferred diameter. The openings 222 have a diameter in the range of 0.1 mm to 6 mm, with 1-3 mm being the preferred diameter range. It is appreciated that although the channels 215 and openings 222 are shown having a generally rounded configuration, it is within the scope of the present invention that the channels 215 and openings 222 may have any size, shape, configuration, and distribution suitable for the intended purpose.

The implant 200, has a plurality of ratchetings 250 on the upper and lower surface 212 and 214 for engaging the bone of the adjacent vertebrae. The ratchetings 250 comprise a bone engaging edge 252 and angled segment 254.

Referring specifically to FIG. 9, the implant 200 has a wedge-shaped elevational side view in which the trailing end 230 is taller than the insertion end 220. The plurality of ratchetings 250 are oriented in the direction of the insertion end 220 to provide for a one-way insertion of the implant 200 as the bone engaging edge 252, or ridge, engages the vertebrae and prevents the implant from backing out once implanted. Alternatively, the trailing end ratchetings could be of a lessor height such that the overall shape of the ratchetings as a group is convex.

Referring to FIG. 11, the trailing end 230 of implant 200 has means for engaging insertion instrumentation comprising a thread opening 226 as described above for implant 100.

Referring to FIG. 12, an enlarged fragmentary view along line 12 of FIG. 8 illustrating the surface configuration the implant 200 is shown. The upper and lower surfaces 212 and 214 of implant 200, in addition to the ratcheting 250 comprise a porous texture 260 to present an irregular surface to the bone to promote bone ingrowth. The porous texture 260 is also able to hold fusion promoting materials and provides for an increased surface area to engage the bone in the fusion process and to provide further stability. The porous texture 260 may also be present on the side walls 218. It is appreciated that the outer surface and/or the entire implant 200, may comprise any other porous material or roughened surface sufficient to hold fusion promoting substances and/or allow for bone ingrowth and/or engage the bone during the fusion process. The implant 200 may be further coated with bioactive fusion promoting substances including, but not limited to, hydroxyapatite compounds, osteogenic proteins and bone morphogenic proteins or may be from bioabsorbable material.

Referring to FIGS. 13-17, an alternative embodiment of the lordotic interbody spinal fusion implant, generally referred to by the numeral 300, is shown. The implant 300 is made of a mesh-like material comprising strands, which may be made of metal, that are pressed together and molded. The upper and lower surfaces 312 and 314 may be convex and conform to the natural surface curvature of the end plates of the vertebrae. In addition, the entire implant 300 may be molded to a shape that conforms to the shape of the disc space created by the removal of disc material from between two adjacent vertebrae. In this manner, the implant 300 has curved upper and lower surfaces 312 and 314, a curved side wall 318 and chamfered edges 319.

Referring to FIG. 7A, the implant 300 is shown inserted in the direction of arrow A into the disc space D1 between adjacent vertebrae V1 and V2. The implant 300 conforms to the endplates of the adjacent vertebrae V1 and V2 as the upper and lower surfaces 312 and 314 are convex, and the side walls 318 are curved to conform to the natural curvature of the vertebrae V1 and V2. In this manner, the implant 300 has the same dimensions as the disc material removed from between the two adjacent vertebrae V1 and V2.

The implant 300 may be made wholly or in part of a solid material and/or a porous material, and/or a mesh-like material. The implant 300 may have a surface comprising of a porous material, a mesh-like material, or have a surface that is roughened. It is appreciated that the implant 300 may be solid or may be partially hollow and include at least one internal chamber in communication with said upper and lower surfaces.

As shown in FIG. 17, the mesh-like material comprises strands that are formed and pressed together such that interstices 339, capable of retaining fusion promoting material and for allowing for bone ingrowth, are present between the strands in at least the outer surface of implant 300. Alternatively, it is appreciated that the implant 300 may be made of a cancellous material, similar in configuration to human cancellous bone, having interstices allowing for bone ingrowth. As the implant 300 may be made entirely or in part of the cancellous material, the interstices may be present in the outer surface of the implant 300 and/or within the entire implant to promote bone ingrowth and hold bone fusion promoting materials.

Referring to FIGS. 18-23 an alternative embodiment of the implant of the present invention, generally referred to by the numeral 400, is disclosed. The implant 400 has a substantially rectangular shape having upper and lower surfaces 412 and 414. The upper and lower surfaces 412 and 414 support the adjacent vertebrae and are disposed in a converging angular relationship to each other in the same manner described above.

The implant 400 has a width W that is substantially less than the width of the implants 100-300 such that a series of such implants 400 are used as the interbody spinal implant, each placed closely adjacent to one another to approximate the size of the removed disc. The size of the implant 400 is approximately 26 millimeters in length and is wide enough so that four of them will substantially fill the intervertebral space, depending on which vertebrae are fused.

In the performing of a posterior lumbar interbody fusion, it is not possible to replace the removed portions of the disc, if a total nuclear discectomy has been performed, with a single large implant as the delicate dural sac containing the spinal cord and nerve roots covers at all times at least some portion of the posterior disc space. The use of modular implants 400 that are inserted separately into the disc space is appropriate in such case. The modular implants 400 being approximately as long as the depth of the disc material removed, but being considerably narrower, such that they could be introduced into the disc space from the posterior aspect to either side of the dural sac, and then realigned side to side with the disc space so that a number of them each having a length consistent with the depth of the disc removed in that area would in combination have a width equal to the width of the disc material removed. As the disc spaces in the lumbar spine are generally lordotic, the insertion end 420 of the modular implants 400 would have to be taller and less tall posteriorly at the trailing end 430.

To introduce the modular implant 400 that is taller at its insertion end 420 than the space available at the posterior aspect of the disc space, even when that disc space is optimally distracted, is problematic. The modular implants 400 of provide two solutions to the problem. The modular implants 400 may have a reduced size at their insertion end 420, including but not limited to, a bullet nose, a convexity, and a chamfer to a smaller front surface. This then provides that the implant 400 has an area small enough to be introduced into the posterior aspect of the disc space when the disc space is adequately distracted and the contour of that specialized insertion end of the implant 400 is such that it then allows for a ramping up of the adjacent vertebrae relative to the implant 400 as the implant is advanced forward into the disc space.

Alternatively, or in combination with the above, since in the preferred embodiment the implants 400 are wedge-shaped in the side elevational view when upright but are generally rectangular when viewed from the top plan view, these implants may be introduced into the disc space on their side such that the side walls of the implants are adjacent to the end plates of the adjacent vertebrae. The implants 400 have a side-to-side dimension that is less than the dimension through the insertion end of the implant 400 when upright. It is possible to easily insert the implant 400 first on their side and then to use the insertion instrument engaged to the implant 400 to rotate the implant ninety degrees into the fully upright position, once it has been fully inserted. Once inserted, the upper and lower surfaces 412 and 414 are adjacent to the endplates of the adjacent vertebrae and create and maintain the desired angular relationship of the adjacent vertebrae as the upper and lower surfaces 412 and 414 of the implant 400 are angled with respect to each other.

The implant 400 has large openings 415 in the form of rectangular slots for holding fusion promoting materials to promote bone growth from the vertebrae through the upper and lower surfaces 412 and 414 and into the interior of the implant 400. As the implant 400 is modular and more than one is implanted at a time, the large openings 415 are also present in the side walls 418 of the implant 400 to provide for bone growth from one implant to another implant such that after successful fusion, the modular implants 400 are interconnected to form a single unit.

Referring to FIG. 21, the trailing end 430 of the implant 400 is shown having an insertion instrument engaging means comprising a rectangular slot 424 and threaded opening 426.

Referring to FIG. 23, an enlarged fragmentary view along line 23 of FIG. 22 illustrating the surface configuration the implant 400 is shown. The surface configuration of the implant 400 is the same as the porous texture 260 described above.

Referring to FIG. 24, an alternative embodiment of the lordotic interbody spinal fusion implant of the present invention, generally referred to by the numeral 500, is shown. The implant 500 is a modular implant and has a similar overall configuration as implant 400. The implant 500 instead of having slots 415 has an upper and lower surfaces 512 and 514 that are capable of receiving and holding bone, or other materials capable of participating in the fusion process and/or capable of promoting bone ingrowth. In the preferred embodiment, the upper and lower surfaces 512 and 514 comprise a plurality of posts 540 that are spaced apart to provide a plurality of interstices 542 which are partial wells with incomplete walls capable of holding and retaining milled bone material or any artificial bone ingrowth promoting material. The implant 500 may be prepared for implantation by grouting or otherwise coating the surface 538 with the appropriate fusion promoting substances.

Referring to FIGS. 28 and 29, an enlarged view of the upper surface 512 of the implant 500 and a partial cross section thereof are shown. In the preferred embodiment, the posts 540 have a head portion 544 of a larger diameter than the remainder of the posts 540, and each of the interstices 542 is the reverse configuration of the posts 544, having a bottom 546 that is wider than the entrance 548 to the interstices 542. Such a configuration of the posts 540 and interstices 542 aids in the retention of bone material in the surface 538 of the implant 500 and further assists in the locking of the implant 500 into the bone fusion mass created from the bone ingrowth. As the bone ingrowth at the bottom 546 of the interstices 542 is wider than the entrance 548, the bone ingrowth cannot exit from the entrance 548 and is locked within the interstice 542. The surface 538 of the implant 500 provides for an improvement in the available amount of surface area which may be still further increased by rough finishing, flocking or otherwise producing a non smooth surface.

In the preferred embodiment, the posts 540 have a maximum diameter in the range of approximately 0.1-2 mm and a height of approximately 0.1-2 mm and are spaced apart a distance of approximately 0.1-2 mm such that the interstices 542 have a width in the range of approximately 0.1 to 2 mm. The post sizes, shapes, and distributions may be varied within the same implant.

It is appreciated that the implant 500 shares the same structure and features of the implant 400 described above.

FIG. 30 is a side elevational view of a segment of the human spinal column S shown in lordosis with an alternative embodiment of the lordotic spinal fusion implant referred to by the numeral 600, that is adjustable and expandable shown inserted in a space to restore and maintain the correct anatomical alignment of the adjacent vertebrae. The implant 600 comprises a lower member 682 and an upper member 684 which when fitted together form an essentially rectangular implant. The upper member 684 and the lower member 682 have hollow portions that face one another and receive tapered wedges 686 and 688 that fit within the hollow portion of the upper and lower members 682 and 684. The upper and lower members 682 and 684 each have a wedged interior surface 689a and 689b which are angled towards the interior of the implant 600. The wedges 682 and 684 are such that at their large end, they are higher than the combined hollow space between the upper and lower members 684 and 682, and shallower at the other end than the hollow space between the upper and lower members.

The wedges 686 and 688 have a central threaded opening 690 and 692 in alignment with each other for receiving threaded screw 694. As the screw 694 is threaded into the opening 690, the wedges 686 and 688 abut the interior sloped surfaces 689a and 689b of the upper and lower members 682 and 684. As the screw 694 is turned, the wedges 686 and 688 are drawn together, and the sloped portions of the wedges force the upper member 682 away from the lower member 684. As the interior sloped surfaces 689a and 689b have a greater slope near the trailing end 630, than near the insertion end 620, the upper and lower members 682 and 684 are forced apart more at the insertion end 620 than at the trailing end 630. As a result, the upper and lower members 682 and 684 are disposed at a converging angular relationship to each other and support the adjacent vertebrae V1 and V2 in the same angular relationship.

Referring to FIG. 31, an alternative embodiment of the implant of the present invention, generally referred to by the numeral 700, is shown. The implant 700 has movable projections, in the form of spikes 708, which are movable from a first position within the implant 700 to a second position extending outside of the implant. The implant 700 is of a generally rectangular configuration, having a top surface 702 and a bottom surface 704 of the implant with slots 706 for permitting pivotal member 707 having spikes 708 at their ends to project through said slots 706. The spikes 708 are pinned at one end 710 within the implant 700.

The implant 700 has opposing wedge shaped members 712 and 714 having a central threaded opening 716 for receiving a threaded screw 718 having a head 720 and a slot 722. The wedges 712 and 714 are facing each other so that upon turning of the screw 718, will the two wedges 712 and 714 are drawn together to cause the spikes 708 to pivot about their end 710 and project to the exterior of the implant 700 through the aligned slots 706. The implant 700 may comprise a series of holes 724 on its surfaces for promoting bone ingrowth and fusion.

In use, after the removal of the disc material, the implant 700 with the spikes 708 in their withdrawn position, is inserted into the disc space. Then the screw 718 is turned until the spikes 708 are forced to enter the vertebrae and the implant 700 is thus held firmly in place.

While the invention has been described with regards to the preferred embodiment and a number of alternative embodiments, it is recognized that other embodiments of the present invention may be devised which would not depart from the scope of the present invention.

Michelson, Gary Karlin

Patent Priority Assignee Title
10058433, Jul 26 2012 DePuy Synthes Products, Inc. Expandable implant
10070968, Aug 24 2010 Flexmedex, LLC Support device and method for use
10070970, Mar 14 2013 SPINE HOLDINGS, LLC Interbody implants and graft delivery systems
10085843, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10085854, Dec 26 2008 Pantheon Spinal, LLC Method of retroperitoneal lateral insertion of spinal implants
10154909, May 16 2013 LDR Medical Vertebral implant, vertebral fastening device of the implant and implant instrumentation
10159582, Sep 16 2011 DePuy Synthes Products, Inc. Removable, bone-securing cover plate for intervertebral fusion cage
10179054, May 22 2008 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Spinal fusion cage system with inserter
10188528, Feb 16 2007 LDR Medical Interveterbral disc prosthesis insertion assemblies
10195046, Dec 31 2009 LDR Medical Instruments and methods for removing fixation devices from intervertebral implants
10195053, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Bone graft delivery system and method for using same
10201355, Feb 06 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Angled surgical tool for removing tissue from within an intervertebral space
10219915, May 22 2013 NuVasive, Inc. Expandable fusion implant and related methods
10226355, Dec 22 2004 LDR Medical Intervertebral disc prosthesis
10238382, Mar 26 2012 ENGAGE MEDICAL HOLDINGS, LLC Blade anchor for foot and ankle
10238426, Jan 23 2012 ENGAGE MEDICAL HOLDINGS, LLC Blade fixation for ankle fusion and arthroplasty
10238500, Jun 27 2002 DePuy Synthes Products, Inc. Intervertebral disc
10245090, Nov 01 2011 ENGAGE MEDICAL HOLDINGS, LLC Blade anchor systems for bone fusion
10245156, Feb 24 2012 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
10245157, Jan 30 2014 LDR Medical Anchoring device for a spinal implant, spinal implant and implantation instrumentation
10245159, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Bone graft delivery system and method for using same
10285819, Nov 12 2008 Stout Medical Group, L.P. Fixation device and method
10285820, Nov 12 2008 Stout Medical Group, L.P. Fixation device and method
10292828, Nov 12 2008 Stout Medical Group, L.P. Fixation device and method
10327911, Jun 24 2010 DePuy Synthes Products, Inc. Enhanced cage insertion assembly
10342667, Dec 16 2010 ENGAGE MEDICAL HOLDINGS, LLC Arthroplasty systems and methods
10342675, Mar 11 2013 STRYKER EUROPEAN HOLDINGS III, LLC Expandable implant
10350083, Feb 24 2012 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
10369015, Sep 23 2010 DEPUY SYNTHES PRODUCTS, INC Implant inserter having a laterally-extending dovetail engagement feature
10376372, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10390955, Sep 22 2016 ENGAGE MEDICAL HOLDINGS, LLC Bone implants
10390963, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
10398563, May 08 2017 MEDOS INTERNATIONAL SARL Expandable cage
10398566, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
10398574, Feb 16 2007 LDR Medical Intervertebral disc prosthesis insertion assemblies
10405986, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10420651, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10433881, Mar 06 2004 DePuy Synthes Products, Inc. Dynamized interspinal implant
10433971, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10433974, Jun 30 2003 DePuy Synthes Products, Inc. Intervertebral implant with conformable endplate
10433977, Jan 17 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant and associated method of manufacturing the same
10449056, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
10449058, Jan 17 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant and associated method of manufacturing the same
10456272, Mar 03 2017 ENGAGE UNI LLC Unicompartmental knee arthroplasty
10478310, May 06 2014 LDR Medical, S.A.S. Vertebral implant, device for vertebral attachment of the implant and instrumentation for implantation thereof
10492918, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10492919, Sep 23 2005 LDR Medical Intervertebral disc prosthesis
10492924, Aug 09 2013 NuVasive, Inc. Lordotic expandable interbody implant
10500062, Dec 10 2009 DePuy Synthes Products, Inc. Bellows-like expandable interbody fusion cage
10512489, Mar 06 2004 DePuy Synthes Products, Inc. Dynamized interspinal implant
10531961, Dec 31 2009 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
10537436, Nov 01 2016 DEPUY SYNTHES PRODUCTS, INC Curved expandable cage
10543107, Dec 07 2009 Devices and methods for minimally invasive spinal stabilization and instrumentation
10548740, Oct 25 2016 Devices and methods for vertebral bone realignment
10548741, Jun 29 2010 DePuy Synthes Products, Inc. Distractible intervertebral implant
10555817, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10575959, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10575961, Sep 23 2011 Spinal fixation devices and methods of use
10583013, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10583015, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
10603185, Feb 04 2004 LDR Medical Intervertebral disc prosthesis
10610380, Dec 07 2009 Devices and methods for minimally invasive spinal stabilization and instrumentation
10617293, Dec 05 2008 Jeffrey B., Kleiner Method and apparatus for performing retro peritoneal dissection
10624758, Mar 30 2009 DePuy Synthes Products, Inc. Zero profile spinal fusion cage
10639164, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
10695105, Aug 28 2012 Spinal fixation devices and methods of use
10702391, May 06 2014 LDR Medical, S.A.S. Vertebral implant, device for vertebral attachment of the implant and instrumentation for implantation thereof
10702392, Apr 25 2012 Theken Spine, LLC Expandable support device and method of use
10716553, Apr 19 2017 Pantheon Spinal, LLC Spine surgery retractor system and related methods
10744000, Oct 25 2016 Devices and methods for vertebral bone realignment
10751187, Jun 08 2007 LDR Medical Intersomatic cage, intervertebral prosthesis, anchoring device and implantation instruments
10758289, May 01 2006 STOUT MEDICAL GROUP, L P Expandable support device and method of use
10758363, Feb 15 2006 LDR Medical Transforaminal intersomatic cage for an intervertebral fusion graft and an instrument for implanting the cage
10779953, May 16 2013 LDR Medical Vertebral implant, vertebral fastening device of the implant and implant instrumentation
10786361, Feb 14 2003 DEPUY SYNTHES PRODUCTS, INC In-situ formed intervertebral fusion device and method
10813677, May 01 2006 STOUT MEDICAL GROUP, L P Expandable support device and method of use
10813773, Sep 16 2011 DePuy Synthes Products, Inc. Removable, bone-securing cover plate for intervertebral fusion cage
10857003, Oct 14 2015 Devices and methods for vertebral stabilization
10857004, Dec 07 2009 Devices and methods for minimally invasive spinal stabilization and instrumentation
10888433, Dec 14 2016 DEPUY SYNTHES PRODUCTS, INC Intervertebral implant inserter and related methods
10898344, Aug 16 2011 STRYKER EUROPEAN HOLDINGS III, LLC Expandable implant
10918498, Nov 24 2004 Devices and methods for inter-vertebral orthopedic device placement
10940014, Nov 12 2008 Stout Medical Group, L.P. Fixation device and method
10940016, Jul 05 2017 DEPUY SYNTHES PRODUCTS, INC; MEDOS INTERNATIONAL SARL Expandable intervertebral fusion cage
10945861, Dec 07 2009 Devices and methods for minimally invasive spinal stabilization and instrumentation
10959860, Dec 26 2008 Pantheon Spinal, LLC Method of retroperitoneal lateral insertion of spinal implants
10966840, Jun 24 2010 DePuy Synthes Products, Inc. Enhanced cage insertion assembly
10973648, Oct 25 2016 Devices and methods for vertebral bone realignment
10973652, Jun 26 2007 DePuy Synthes Products, Inc. Highly lordosed fusion cage
10973656, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Bone graft delivery system and method for using same
11006982, Feb 22 2012 Spinous process fixation devices and methods of use
11026806, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
11051954, Sep 21 2004 Stout Medical Group, L.P. Expandable support device and method of use
11058548, Oct 25 2016 Samy, Abdou Devices and methods for vertebral bone realignment
11096794, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
11096796, May 06 2005 Titan Spine, LLC Interbody spinal implant having a roughened surface topography on one or more internal surfaces
11096799, Nov 24 2004 Devices and methods for inter-vertebral orthopedic device placement
11129730, May 22 2008 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Spinal fusion cage system with inserter
11141208, May 01 2006 STOUT MEDICAL GROUP, L P Expandable support device and method of use
11173040, Oct 22 2012 Cogent Spine, LLC Devices and methods for spinal stabilization and instrumentation
11173043, May 17 2019 Spinal interbody implants
11179248, Oct 02 2018 Samy, Abdou Devices and methods for spinal implantation
11197763, Dec 16 2010 ENGAGE MEDICAL HOLDINGS, LLC Arthroplasty systems and methods
11207187, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
11246715, Dec 31 2009 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
11246718, Oct 14 2015 Devices and methods for vertebral stabilization
11259935, Oct 25 2016 Devices and methods for vertebral bone realignment
11273050, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
11273056, Feb 24 2012 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
11324608, Sep 23 2011 Spinal fixation devices and methods of use
11344424, Jun 14 2017 MEDOS INTERNATIONAL SARL Expandable intervertebral implant and related methods
11364057, Mar 27 2009 Spinal Elements, Inc. Flanged interbody fusion device
11369488, Mar 03 2017 ENGAGE UNI LLC Unicompartmental knee arthroplasty
11382769, Sep 20 2018 SPINAL ELEMENTS, INC Spinal implant device
11426286, Mar 06 2020 EIT Emerging Implant Technologies GmbH Expandable intervertebral implant
11426290, Mar 06 2015 SYNTHES USA PRODUCTS, LLC; DEPUY SYNTHES PRODUCTS, INC Expandable intervertebral implant, system, kit and method
11432938, Feb 14 2003 DEPUY SYNTHES PRODUCTS, INC In-situ intervertebral fusion device and method
11432942, Dec 07 2006 DEPUY SYNTHES PRODUCTS, INC Intervertebral implant
11446155, May 08 2017 MEDOS INTERNATIONAL SARL Expandable cage
11446156, Oct 25 2018 MEDOS INTERNATIONAL SARL Expandable intervertebral implant, inserter instrument, and related methods
11452607, Oct 11 2010 DePuy Synthes Products, Inc. Expandable interspinous process spacer implant
11452609, Mar 30 2009 DePuy Synthes Products, Inc. Zero profile spinal fusion cage
11478237, Apr 19 2017 Pantheon Spinal, LLC Spine surgery retractor system and related methods
11497618, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
11497619, Mar 07 2013 DePuy Synthes Products, Inc. Intervertebral implant
11510788, Jun 28 2016 EIT Emerging Implant Technologies GmbH Expandable, angularly adjustable intervertebral cages
11517449, Sep 23 2011 Spinal fixation devices and methods of use
11534312, Apr 25 2012 Theken Spine, LLC Expandable support device and method of use
11540928, Mar 03 2017 ENGAGE UNI LLC; ENGAGE UNI LLC DBA ENGAGE SURGICAL Unicompartmental knee arthroplasty
11554020, Sep 08 2020 Life Spine, Inc Expandable implant with pivoting control assembly
11559336, Aug 28 2012 Spinal fixation devices and methods of use
11596522, Jun 28 2016 EIT Emerging Implant Technologies GmbH Expandable and angularly adjustable intervertebral cages with articulating joint
11596523, Jun 28 2016 EIT Emerging Implant Technologies GmbH Expandable and angularly adjustable articulating intervertebral cages
11602438, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
11602439, Apr 16 2020 Life Spine, Inc Expandable implant assembly
11602440, Jun 25 2020 Life Spine, Inc Expandable implant assembly
11607321, Dec 10 2009 DePuy Synthes Products, Inc. Bellows-like expandable interbody fusion cage
11612491, Mar 30 2009 DePuy Synthes Products, Inc. Zero profile spinal fusion cage
11612493, Jun 30 2003 DePuy Synthes Products, Inc. Intervertebral implant with conformable endplate
11617655, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
11622868, Jun 26 2007 DePuy Synthes Products, Inc. Highly lordosed fusion cage
11633288, May 16 2013 LDR Medical Vertebral implant, vertebral fastening device of the implant and implant instrumentation
11642229, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
11648131, Aug 16 2011 Stryker European Operations Holdings LLC Expandable implant
11654033, Jun 29 2010 DePuy Synthes Products, Inc. Distractible intervertebral implant
11660206, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
11660208, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC. Bone graft delivery system and method for using same
11666455, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Bone graft delivery devices, systems and kits
11696836, Aug 09 2013 NuVasive, Inc. Lordotic expandable interbody implant
11701234, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
11707359, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
11712341, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
11712342, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
11712345, Dec 07 2006 DePuy Synthes Products, Inc. Intervertebral implant
11737881, Jan 17 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant and associated method of manufacturing the same
11737884, Jun 23 2016 VGI Medical, LLC Method and apparatus for spinal facet fusion
11752008, Oct 25 2016 Devices and methods for vertebral bone realignment
11752009, Apr 06 2021 MEDOS INTERNATIONAL SARL Expandable intervertebral fusion cage
11806245, Mar 06 2020 EIT Emerging Implant Technologies GmbH Expandable intervertebral implant
11839413, Feb 22 2012 Spinous process fixation devices and methods of use
11850160, Mar 26 2021 MEDOS INTERNATIONAL SARL Expandable lordotic intervertebral fusion cage
11850164, Mar 07 2013 DePuy Synthes Products, Inc. Intervertebral implant
11857432, Apr 13 2020 Life Spine, Inc Expandable implant assembly
11872138, Sep 23 2005 LDR Medical Intervertebral disc prosthesis
11872139, Jun 24 2010 DePuy Synthes Products, Inc. Enhanced cage insertion assembly
11872143, Oct 25 2016 Camber Spine Technologies, LLC Spinal fusion implant
11877935, Oct 18 2016 Camber Spine Technologies, LLC Implant with deployable blades
11896494, Jul 10 2017 Life Spine, Inc Expandable implant assembly
11911284, Nov 19 2020 SPINAL ELEMENTS, INC Curved expandable interbody devices and deployment tools
11911287, Jun 24 2010 DePuy Synthes Products, Inc. Lateral spondylolisthesis reduction cage
7871441, Apr 28 2006 SPINAL ELEMENTS, INC Cervical fixation device
7935148, Jan 09 2006 Warsaw Orthopedic, Inc Adjustable insertion device for a vertebral implant
8021430, Jun 07 1995 Warsaw Orthopedic, Inc. Anatomic spinal implant having anatomic bearing surfaces
8088163, Feb 06 2008 NuVasive, Inc Tools and methods for spinal fusion
8137402, Jan 17 2002 SPINAL ELEMENTS, INC Vertebral defect device
8147547, Apr 29 2005 Warsaw Orthopedic, Inc Spinal implant
8162981, May 22 2007 VG Innovations, LLC Method and apparatus for spinal facet fusion
8167886, Jan 17 2002 SPINAL ELEMENTS, INC Insertion tool for a vertebral defect device
8257439, Dec 22 2004 LDR Medical Intervertebral disc prosthesis
8262737, May 06 2005 Titan Spine, LLC Composite interbody spinal implant having openings of predetermined size and shape
8267999, Nov 05 2002 LDR Medical Intervertebral disc prosthesis
8277510, Feb 06 2009 Kleiner Intellectual Property, LLC Tools and methods for spinal fusion
8292960, Feb 06 2008 NuVasive, Inc Spinal fusion cage with removable planar elements
8313528, Mar 27 2008 SPINELOGIK, INC Intervertebral fusion device and method of use
8333804, Mar 27 2008 SPINELOGIK, INC Intervertebral fusion device and method of use
8343219, Jun 08 2007 LDR Medical Intersomatic cage, intervertebral prosthesis, anchoring device and implantation instruments
8353962, Apr 28 2006 SPINAL ELEMENTS, INC Dual composition vertebral defect device
8366748, Dec 05 2008 Apparatus and method of spinal implant and fusion
8382839, Mar 27 2008 SPINELOGIK, INC Intervertebral fusion device and method of use
8403991, May 06 2005 Titan Spine LLC Implant with critical ratio of load bearing surface area to central opening area
8409290, Mar 08 2006 SEASPINE, INC. Interbody device for spinal applications
8435302, May 06 2005 Titan Spine, LLC Instruments and interbody spinal implants enhancing disc space distraction
8444696, Jun 07 1995 Warsaw Orthopedic, Inc. Anatomic spinal implant having anatomic bearing surfaces
8460385, Mar 27 2008 SPINELOGIK, INC Fusion member for insertion between vertebral bodies
8465546, Feb 16 2007 LDR Medical Intervertebral disc prosthesis insertion assemblies
8480749, May 06 2005 Titan Spine, LLC Friction fit and vertebral endplate-preserving spinal implant
8496710, May 06 2005 Titan Spine, LLC Interbody spinal implant having a roughened surface topography
8523945, Mar 27 2008 SPINELOGIK, INC Method and apparatus for affixing a fusion member to vertebral bodies
8535380, May 13 2010 STOUT MEDICAL GROUP, L P Fixation device and method
8545568, May 06 2005 Titan Spine, LLC Method of using instruments and interbody spinal implants to enhance distraction
8551175, Mar 27 2008 SPINELOGIK, INC Method and apparatus for retaining a fusion member while delivering the fusion member between two vertebral bodies
8551176, May 06 2005 Titan Spine, LLC Spinal implant having a passage for enhancing contact between bone graft material and cortical endplate bone
8562684, May 06 2005 Titan Spine, LLC Endplate-preserving spinal implant with an integration plate having a roughened surface topography
8562685, May 06 2005 Titan Spine, LLC Spinal implant and integration plate for optimizing vertebral endplate contact load-bearing edges
8585765, May 06 2005 Titan Spine, LLC Endplate-preserving spinal implant having a raised expulsion-resistant edge
8585766, May 06 2005 Titan Spine, LLC Endplate-preserving spinal implant with an integration plate having durable connectors
8585767, May 06 2005 Titan Spine, LLC Endplate-preserving spinal implant with an integration plate having durable connectors
8591590, May 06 2005 Titan Spine, LLC Spinal implant having a transverse aperture
8617248, May 06 2005 Titan Spine, LLC Spinal implant having variable ratios of the integration surface area to the axial passage area
8673012, Mar 08 2006 SEASPINE, INC. Intervertebral spacer and insertion tool providing multiple angles of insertion
8685031, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Bone graft delivery system
8709042, Sep 21 2004 STOUT MEDICAL GROUP, L P Expandable support device and method of use
8709088, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Fusion cage with combined biological delivery system
8715355, Feb 06 2008 NuVasive, Inc Spinal fusion cage with removable planar elements
8728164, Aug 25 2004 BUCK GMBH & CO , KG Implant for surgical use in humans or vertebrates
8734493, Sep 30 2003 X-spine Systems, Inc. Screw locking mechanism and method
8758442, May 06 2005 Titan Spine, LLC Composite implants having integration surfaces composed of a regular repeating pattern
8758443, May 06 2005 Titan Spine, LLC Implants with integration surfaces having regular repeating surface patterns
8771284, Nov 30 2005 LDR Medical Intervertebral disc prosthesis and instrumentation for insertion of the prosthesis between the vertebrae
8795370, Sep 30 2003 X-spine Systems, Inc. Fusion system and method for fusing spinal bones
8795375, Jul 23 2008 ResSpond Spinal Systems Modular nucleus pulposus prosthesis
8808305, May 22 2008 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Spinal fusion cage system with inserter
8814939, May 06 2005 Titan Spine, LLC Implants having three distinct surfaces
8821553, Sep 30 2003 X-spine Systems, Inc.; X-SPINE SYSTEMS, INC Spinal fusion system utilizing an implant plate having at least one integral lock
8834571, May 06 2005 Titan Spine, LLC Interbody spinal implant having a roughened surface topography
8858635, Feb 04 2004 LDR Medical Intervertebral disc prosthesis
8858638, Jun 07 1995 Warsaw Orthopedic, Inc. Spinal implant
8864654, Apr 20 2010 KLEINER, JEFFREY B Method and apparatus for performing retro peritoneal dissection
8870882, Dec 05 2008 Apparatus and method of spinal implant and fusion
8906028, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Bone graft delivery device and method of using the same
8940053, May 06 2005 Titan Spine, LLC Spinal implant and integration plate for optimizing vertebral endplate contact load-bearing edges
8974532, Apr 28 2004 LDR Medical Intervertebral disc prosthesis
8979932, Sep 23 2005 LDR Medical Intervertebral disc prosthesis
8992619, Nov 01 2011 Titan Spine LLC Microstructured implant surfaces
8992622, May 06 2005 Titan Spine, LLC Interbody spinal implant having a roughened surface topography
9011546, May 06 2005 Titan Spine, LLC Composite implants having integration surfaces composed of a regular repeating pattern
9028549, Mar 27 2008 SPINELOGIK, INC. Intervertebral fusion device and method of use
9039774, Feb 24 2012 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
9044337, Dec 31 2009 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
9050112, Aug 23 2011 Flexmedex, LLC Tissue removal device and method
9060877, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Fusion cage with combined biological delivery system
9078706, Sep 30 2003 X-spine Systems, Inc. Intervertebral fusion device utilizing multiple mobile uniaxial and bidirectional screw interface plates
9078765, Jul 13 2001 LDR Medical Vertebral cage device with modular fixation
9095385, Nov 21 2012 K2M, INC Adjustable spinal implant insertion instrument
9125756, May 06 2005 Titan Spine, LLC Processes for producing regular repeating patterns on surfaces of interbody devices
9149286, Nov 12 2010 Flexmedex, LLC Guidance tool and method for use
9168147, May 06 2005 Titan Spine, LLC Self-deploying locking screw retention device
9173694, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Fusion cage with combined biological delivery system
9186193, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Fusion cage with combined biological delivery system
9216096, Mar 16 2010 SPINE HOLDINGS, LLC Intervertebral implants and related tools
9247943, Feb 06 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Devices and methods for preparing an intervertebral workspace
9254130, Nov 01 2011 ENGAGE MEDICAL HOLDINGS, LLC Blade anchor systems for bone fusion
9259329, Sep 21 2004 Stout Medical Group, L.P. Expandable support device and method of use
9295562, Jan 17 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant and associated method of manufacturing the same
9314349, Sep 21 2004 STOUT MEDICAL GROUP, L P Expandable support device and method of use
9320610, Aug 16 2011 STRYKER EUROPEAN HOLDINGS III, LLC Expandable implant
9320615, Jun 29 2010 DEPUY SYNTHES PRODUCTS, INC Distractible intervertebral implant
9327051, May 06 2005 Titan Spine, LLC Implants with integration surfaces having regular repeating surface patterns
9333095, May 04 2001 LDR Medical Intervertebral disc prosthesis, surgical methods, and fitting tools
9358122, Jan 07 2011 SOO, TEK Interbody spacer
9364338, Jul 23 2008 ResSpond Spinal Systems Modular nucleus pulposus prosthesis
9380932, Nov 02 2011 SPINE HOLDINGS, LLC Retractor devices for minimally invasive access to the spine
9402737, Jun 26 2007 DePuy Synthes Products, Inc. Highly lordosed fusion cage
9414934, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
9427264, Dec 05 2008 Apparatus and method of spinal implant and fusion
9427324, Feb 22 2010 SPINELOGIK, INC Intervertebral fusion device and method of use
9433510, Jan 17 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant and associated method of manufacturing the same
9433511, May 06 2005 Titan Spine, LLC Interbody spinal implant having a roughened surface topography
9439782, May 22 2008 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Spinal fusion cage system with inserter
9451940, Dec 26 2008 Pantheon Spinal, LLC Method of retroperitoneal lateral insertion of spinal implants
9463091, Sep 17 2009 ZIMMER BIOMET SPINE, INC ; ZIMMER CEP USA HOLDING CO Intervertebral implant having extendable bone fixation members
9474623, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
9480511, Jan 23 2012 ENGAGE MEDICAL HOLDINGS, LLC Blade fixation for ankle fusion and arthroplasty
9498349, Oct 09 2012 Titan Spine, LLC Expandable spinal implant with expansion wedge and anchor
9526620, Mar 30 2009 DEPUY SYNTHES PRODUCTS, INC Zero profile spinal fusion cage
9526625, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
9545314, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
9561117, Jul 26 2012 DePuy Synthes Products, Inc. Expandable implant
9579215, Jun 29 2010 DePuy Synthes Products, Inc. Distractible intervertebral implant
9592129, Mar 30 2009 DePuy Synthes Products, Inc. Zero profile spinal fusion cage
9597195, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
9615935, Jan 30 2014 Titan Spine, LLC Thermally activated shape memory spring assemblies for implant expansion
9622876, Apr 25 2012 Theken Spine, LLC Expandable support device and method of use
9629729, Sep 18 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Biological delivery system with adaptable fusion cage interface
9642721, Oct 02 2012 Titan Spine, LLC Implants with self-deploying anchors
9649203, Mar 16 2010 SPINE HOLDINGS, LLC Methods of post-filling an intervertebral implant
9655745, May 06 2005 Titan Spine, LLC Methods for manufacturing implants having integration surfaces
9675389, Dec 07 2009 Stryker European Operations Limited Devices and methods for minimally invasive spinal stabilization and instrumentation
9707100, Jun 25 2015 Camber Spine Technologies, LLC Interbody fusion device and system for implantation
9713535, Feb 15 2006 LDR Medical Transforaminal intersomatic cage for an intervertebral fusion graft and an instrument for implanting the cage
9717403, Dec 05 2008 Jeffrey B., Kleiner Method and apparatus for performing retro peritoneal dissection
9717600, Mar 27 2008 SPINELOGIK, INC Bioabsorbable anchoring member for insertion into a vertebral body
9717601, Feb 28 2013 DEPUY SYNTHES PRODUCTS, INC Expandable intervertebral implant, system, kit and method
9724207, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9730805, Mar 27 2008 SPINELOGIK, INC. Intervertebral fusion device and method or use
9750552, Jul 06 2009 DePuy Synthes Products, Inc. Expandable fixation assemblies
9770339, Jul 14 2005 Stout Medical Group, L.P. Expandable support device and method of use
9782271, Feb 28 2008 STRYKER EUROPEAN HOLDINGS III, LLC Expandable intervertebral implant
9788963, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9788971, May 22 2013 NuVasive, Inc Expandable fusion implant and related methods
9788973, Mar 16 2010 SPINE HOLDINGS, LLC Spinal implant
9801729, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9801734, Aug 09 2013 NuVasive, Inc Lordotic expandable interbody implant
9808351, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9814589, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9814590, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9826988, Feb 06 2009 SPINAL SURGICAL STRATEGIES, INC , A NEVADA CORPORATION D B A KLEINER DEVICE LABS Devices and methods for preparing an intervertebral workspace
9833331, Dec 31 2009 LDR Medical Anchoring device and system for an intervertebral implant, intervertebral implant and implantation instrument
9833334, Jun 24 2010 DePuy Synthes Products, Inc. Enhanced cage insertion assembly
9839530, Jun 26 2007 DePuy Synthes Products, Inc. Highly lordosed fusion cage
9848995, Mar 20 2012 Titan Spine LLC Process for fabricating bioactive vertebral endplate bone-contacting surfaces on a spinal implant
9861496, Jun 22 2012 Apparatus and method of spinal implant and fusion
9877842, Jan 30 2014 LDR Medical Anchoring device for a spinal implant, spinal implant and implantation instrumentation
9895236, Jun 24 2010 DePuy Synthes Products, Inc. Enhanced cage insertion assembly
9907654, Dec 11 2012 DR H C ROBERT MATHYS STIFTUNG Bone substitute and method for producing the same
9913727, Jul 02 2015 MEDOS INTERNATIONAL SARL Expandable implant
9925051, Dec 16 2010 ENGAGE MEDICAL HOLDINGS, LLC Arthroplasty systems and methods
9925060, Feb 14 2003 DePuy Synthes Products, Inc. In-situ formed intervertebral fusion device and method
9931223, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
9937050, May 16 2013 LDR Medical Vertebral implant, vertebral fastening device of the implant and implant instrumentation
9949769, Mar 06 2004 DePuy Synthes Products, Inc. Dynamized interspinal implant
9962270, Aug 16 2011 STRYKER EUROPEAN HOLDINGS III, LLC Expandable implant
9974661, May 16 2013 LDR Medical Vertebral implant, vertebral fastening device of the implant and implant instrumentation
9987052, Feb 24 2015 X-SPINE SYSTEMS, INC Modular interspinous fixation system with threaded component
9993349, Jun 27 2002 DEPUY SYNTHES PRODUCTS, INC Intervertebral disc
9993350, Apr 05 2008 DePuy Synthes Products, Inc. Expandable intervertebral implant
D656610, Feb 06 2009 NuVasive, Inc Spinal distraction instrument
D667542, Feb 06 2009 Spinal distraction instrument
D696399, Feb 06 2009 Kleiner Intellectual Property, LLC Spinal distraction instrument
D700322, Oct 20 2011 Intervertebral surgical tool
D723682, May 03 2013 Spinal Surgical Strategies, LLC Bone graft delivery tool
D750249, Oct 20 2014 Spinal Surgical Strategies, LLC Expandable fusion cage
D797290, Oct 19 2015 Spinal Surgical Strategies, LLC Bone graft delivery tool
D853560, Oct 09 2008 NuVasive, Inc. Spinal implant insertion device
Patent Priority Assignee Title
3848601,
3867728,
3875595,
3948262, Apr 01 1969 ALZA Corporation Novel drug delivery device
4309777, Nov 13 1980 Artificial intervertebral disc
4349921, Jun 16 1980 Intervertebral disc prosthesis
4401112, Oct 02 1981 Spinal fixator
4501269, Dec 11 1981 ZIMMER SPINE, INC Process for fusing bone joints
4507115, Apr 01 1981 Olympus Optical Co., Ltd. Medical capsule device
4545374, Sep 03 1982 Method and instruments for performing a percutaneous lumbar diskectomy
4554914, Oct 04 1983 Prosthetic vertebral body
4599086, Jun 07 1985 Spine stabilization device and method
4714469, Feb 26 1987 PFIZER HOSPITAL PRODUCTS GROUP, INC Spinal implant
4721103, Jan 31 1985 Orthopedic device
4743256, Oct 04 1985 DEPUY ACROMED, INC Surgical prosthetic implant facilitating vertebral interbody fusion and method
4759766, Sep 04 1984 WALDEMAR LINK GMBH & CO Intervertebral disc endoprosthesis
4759769, Feb 12 1987 Health & Research Services Inc. Artificial spinal disc
4834757, Oct 04 1985 DEPUY ACROMED, INC Prosthetic implant
4863476, Aug 29 1986 ZIMMER TECHNOLOGY, INC Spinal implant
4863477, May 12 1987 Synthetic intervertebral disc prosthesis
4865603, Feb 04 1988 JOIN MEDICAL PRODUCTS CORPORATION; Joint Medical Products Corporation Metallic prosthetic devices having micro-textured outer surfaces
4878915, Oct 04 1985 DEPUY ACROMED, INC Surgical prosthetic implant facilitating vertebral interbody fusion
4904261, Aug 06 1987 Surgicraft Limited Spinal implants
4911718, Jun 10 1988 UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY, THE Functional and biocompatible intervertebral disc spacer
4936848, Sep 22 1989 ZIMMER SPINE, INC Implant for vertebrae
4955908, Jul 09 1987 Zimmer GmbH Metallic intervertebral prosthesis
4961740, Oct 17 1988 HOWMEDICA OSTEONICS CORP V-thread fusion cage and method of fusing a bone joint
5015247, Jun 13 1988 Warsaw Orthopedic, Inc Threaded spinal implant
5026373, Oct 17 1988 HOWMEDICA OSTEONICS CORP Surgical method and apparatus for fusing adjacent bone structures
5055104, Oct 17 1988 HOWMEDICA OSTEONICS CORP Surgically implanting threaded fusion cages between adjacent low-back vertebrae by an anterior approach
5062845, May 10 1989 ZIMMER SPINE, INC Method of making an intervertebral reamer
5071437, Feb 15 1989 DEPUY ACROMED, INC Artificial disc
5122130, Mar 23 1988 Waldemar Link GmbH & Co. Forceps for inserting intervertebral device
5123926, Feb 22 1991 Perumala Corporation Artificial spinal prosthesis
5171278, Feb 22 1991 Perumala Corporation Middle expandable intervertebral disk implants
5190548, Apr 10 1991 ZIMMER TECHNOLOGY, INC Surgical reamer
5192327, Mar 22 1991 DEPUY ACROMED, INC Surgical prosthetic implant for vertebrae
5246458, Oct 07 1992 Artificial disk
5250061, Sep 08 1988 Codman & Shurtleff, Inc Ring currette
5258031, Jan 06 1992 SDGI Holdings, Inc Intervertebral disk arthroplasty
5258043, Jul 20 1987 ReGen Corporation Method for making a prosthetic intervertebral disc
5304191, Feb 12 1993 MIDAS REX, L P Surgical instrument with rotatable indexing footed attachment
5306308, Oct 23 1989 Intervertebral implant
5306309, May 04 1992 Zimmer Dental, Inc Spinal disk implant and implantation kit
5360430, Jul 29 1993 Intervertebral locking device
5370697, Apr 21 1992 Sulzer Medizinaltechnik AG Artificial intervertebral disk member
5397364, Oct 12 1993 SDGI Holdings, Inc Anterior interbody fusion device
5425772, Sep 20 1993 DEPUY ACROMED, INC Prosthetic implant for intervertebral spinal fusion
5443514, Oct 01 1993 DEPUY ACROMED, INC Method for using spinal implants
5445639, May 10 1989 ZIMMER SPINE, INC Intervertebral reamer construction
5458638, Jul 06 1989 ZIMMER SPINE, INC Non-threaded spinal implant
5458643, Mar 29 1991 BMG Incorporated Artificial intervertebral disc
5484437, Jun 13 1988 Warsaw Orthopedic, Inc Apparatus and method of inserting spinal implants
5489307, Feb 10 1993 ZIMMER SPINE, INC Spinal stabilization surgical method
5499984, Apr 07 1994 ZIMMER TECHNOLOGY, INC Universal modular reamer system
5522899, Jun 28 1988 Warsaw Orthopedic, Inc Artificial spinal fusion implants
5534028, Apr 20 1993 HOWMEDICA OSTEONICS CORP Hydrogel intervertebral disc nucleus with diminished lateral bulging
5554191, Jan 26 1994 Biomat Intersomatic vertebral cage
5571109, Aug 26 1993 SDGI Holdings, Inc System for the immobilization of vertebrae
5571190, Aug 20 1993 Heinrich, Ulrich Implant for the replacement of vertebrae and/or stabilization and fixing of the spinal column
5607424, Apr 10 1995 Domed cage
5609635, Jun 28 1988 Warsaw Orthopedic, Inc Lordotic interbody spinal fusion implants
5609636, May 23 1994 ZIMMER SPINE, INC Spinal implant
5609637, Jul 09 1993 Space keeper, in particular for an intervertebral disk
5653763, Mar 29 1996 ZIMMER SPINE, INC Intervertebral space shape conforming cage device
5658335, Mar 09 1995 ALLEN, RONALD CHARLES, SOLE TRUSTEE, OR HIS SUCCESSORS IN TRUST, UNDER THE RONALD CHARLES ALLEN LIVING TRUST, DATED MARCH 28, 2009, AND ANY AMENDMENTS THERETO Spinal fixator
5658337, May 23 1994 ZIMMER SPINE, INC Intervertebral fusion implant
5665122, Jan 31 1995 Expandable intervertebral cage and surgical method
5669909, Mar 27 1995 SDGI Holdings, Inc Interbody fusion device and method for restoration of normal spinal anatomy
5683463, Aug 06 1993 Advanced Technical Fabrication Intersomatic vertebral column implant
5766252, Jan 24 1995 HOWMEDICA OSTEONICS CORP Interbody spinal prosthetic implant and method
5769897, Dec 13 1991 Synthetic bone
5782919, Mar 27 1995 Warsaw Orthopedic, Inc Interbody fusion device and method for restoration of normal spinal anatomy
5800547, Aug 20 1994 DePuy Spine SARL; MICOMED ORTHO AG Ventral intervertebral implant
5824094, Oct 17 1997 TLIF, LLC Spinal disc
5861041, Apr 07 1997 Arthit Sitiso; Frank Bailly; John Wagner; Pibul, Itiravivong; Somsak, Kuptniratsaikul; Tawechai, Tejapongvorachai; Prakit, Tienboon Intervertebral disk prosthesis and method of making the same
5888224, Sep 21 1993 Synthes USA, LLC Implant for intervertebral space
5888227, Oct 20 1995 Synthes USA, LLC Inter-vertebral implant
5893890, Mar 18 1994 Perumala Corporation Rotating, locking intervertebral disk stabilizer and applicator
5980522, Jul 22 1994 Expandable spinal implants
5984967, Mar 27 1995 Warsaw Orthopedic, Inc Osteogenic fusion devices
6059829, Mar 08 1995 Synthes USA, LLC Intervertebral implant
6149686, Jul 06 1989 ZIMMER SPINE, INC Threaded spinal implant with bone ingrowth openings
6159214, Jul 31 1996 Warsaw Orthopedic, Inc Milling instrumentation and method for preparing a space between adjacent vertebral bodies
6558423, May 05 1999 Warsaw Orthopedic, Inc; SDGI Holdings, Inc Interbody spinal fusion implants with multi-lock for locking opposed screws
6613091, Mar 27 1995 SDGI Holdings, Inc. Spinal fusion implants and tools for insertion and revision
20030149483,
20030233145,
CA1328957,
CA2151481,
D245259, Jan 29 1976 Zimmer U.S.A. Inc. Tibial prosthesis
DE2910627,
DE3620549,
EP179695,
EP260044,
EP425542,
EP493698,
EP599419,
EP627204,
EP646366,
FR2703580,
JP5208029,
JP6031706,
JP6043984,
JP62155846,
SU1107854,
WO9301771,
WO9622747,
WO9000037,
//////
Executed onAssignorAssigneeConveyanceFrameReelDoc
Sep 09 2002Warsaw Orthopedic, Inc.(assignment on the face of the patent)
May 17 2005MICHELSON, GARY KARLINSDGI Holdings, IncASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0161950282 pdf
May 17 2005KARLIN TECHNOLOGY, INC SDGI Holdings, IncASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0161950282 pdf
Apr 28 2006SDGI Holdings, IncWarsaw Orthopedic, IncMERGER SEE DOCUMENT FOR DETAILS 0187570105 pdf
Dec 01 2006SDGI Holdings, IncWarsaw Orthopedic, IncCORRECTIVE ASSIGNMENT TO CORRECT T0 REMOVE APPLICATION NUMBER PREVIOUSLY RECORDED AT REEL: 018573 FRAME: 0086 ASSIGNOR S HEREBY CONFIRMS THE MERGER 0339040891 pdf
Dec 01 2006SDGI Holdings, IncWarsaw Orthopedic, IncMERGER SEE DOCUMENT FOR DETAILS 0185730086 pdf
Date Maintenance Fee Events
Sep 17 2012M1551: Payment of Maintenance Fee, 4th Year, Large Entity.
Oct 28 2016REM: Maintenance Fee Reminder Mailed.
Mar 17 2017EXP: Patent Expired for Failure to Pay Maintenance Fees.


Date Maintenance Schedule
Mar 17 20124 years fee payment window open
Sep 17 20126 months grace period start (w surcharge)
Mar 17 2013patent expiry (for year 4)
Mar 17 20152 years to revive unintentionally abandoned end. (for year 4)
Mar 17 20168 years fee payment window open
Sep 17 20166 months grace period start (w surcharge)
Mar 17 2017patent expiry (for year 8)
Mar 17 20192 years to revive unintentionally abandoned end. (for year 8)
Mar 17 202012 years fee payment window open
Sep 17 20206 months grace period start (w surcharge)
Mar 17 2021patent expiry (for year 12)
Mar 17 20232 years to revive unintentionally abandoned end. (for year 12)